Tag: Nextseq
Rising Demand for Early Cancer Detection is Significantly Contributing to Growth
DUBLIN, June 9, 2023 /PRNewswire/ — The “DNA and Gene Chip Global Market Report 2023” report has been added to ResearchAndMarkets.com‘s offering. This report provides strategists, marketers and senior management with the critical information they need to assess the market. The global DNA and gene chip market is expected to…
Efflux pump gene amplifications bypass necessity of multiple target mutations for resistance against dual-targeting antibiotic
Strains and growth conditions All strains and plasmids used in this work are described in Supplementary Table 1. The clinical isolates were obtained from the Cystic Fibrosis Foundation Isolate Core at Seattle Children’s Hospital and were originally isolated from two different cystic fibrosis patients. Distribution of these isolates is covered by…
acCRISPR: an activity-correction method for improving the accuracy of CRISPR screens
acCRISPR framework acCRISPR performs essential gene identification by calculating two scores for each sgRNA, namely the cutting score (CS) and the fitness score (FS). CS and FS are the log2-fold change of sgRNA abundance in the appropriate treatment sample with respect to that in the corresponding control sample (see Supplementary…
A case report of cutaneous anthrax diagnosed with mNGS
Yushan Liu,1,2 Gezhi Zheng,1,3 Jing Li,1,3 Nan Yang,1– 4 Juan Li,1,2 Zhengwen Liu,1– 4 Qunying Han,1– 4 Yingren Zhao,1– 4 Fenjing Du,1,3 Yingli He,1,* Taotao Yan1,* 1Department of Infectious Diseases, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, Shaanxi, People’s Republic of China; 2Institution of Hepatology, The First Affiliated…
LHH hiring Bioinformatics Scientist in Waltham, Massachusetts, United States
A Bioinformatics Scientist position in Waltham, MA is now available through Adecco Medical and Science. We are seeking a Contract Bioinformatics Scientist to be part of a team focused on cell and genome engineering in the Genomic Medicine Unit. The successful candidate will support the activities around various projects that…
PacBio Pipeline and Tools for Variant Call
PacBio Pipeline and Tools for Variant Call 0 Hi, I am new to long read seq, I am trying to call Variants on GIAB Trio samples from PacBio data Initially i Aligned reads with Pbmm2 tool, then variant call by DeepVariant 1.5, Phasing through Whatshap. My queries are as follows…
Frederick National Laboratory for Cancer Research hiring Bioinformatics Analyst II/III in Frederick, Maryland, United States
Job ID: req3395Employee Type: exempt full-timeDivision: Bioinformatics and Computational ScienceFacility: Frederick: ATRFLocation: 8560 Progress Dr, Frederick, MD 21701 USAThe Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of…
Integrated Resources, Inc ( IRI ) hiring Bioinformatics Scientist in Waltham, Massachusetts, United States
Description: Contract Worker, Bioinformatics, Cell and Genome Engineering, Genomic Medicine Unit We are seeking a contract bioinformatics scientist to be part of a team focused on cell and genome engineering in the Genomic Medicine Unit. The successful candidate will play an important role to support the activities around various projects…
Four MORE Chinese DNA Sequencing Startups
Yesterday I wrote about eight Chinese DNA sequencing companies. Today I found out about 4 more! So let’s very quickly review! Looks like Illumina-style SBS using an unspecified surface amplification approach. According to their website: Q30>85%, run outputs up to 300Gb. Two instruments, the Salus Pro and Salus Evo. Seems…
an extremely low rate of correct barcodes was observed
cellranger count: an extremely low rate of correct barcodes was observed 1 I am new to cellranger. And I tried to run cellranger count for a fastq.gz file. My code is something like this: (** is just to replace my address name due to privacy issue) fastq-dump –outdir fastq –split-files…
Methanol fixation is the method of choice for droplet-based single-cell transcriptomics of neural cells
hiPSC cell culture and differentiation hiPSCs were maintained on 1:40 matrigel (Corning, #354277) coated dishes in supplemented mTeSR-1 medium (StemCell Technologies, #85850) with 500 U ml−1 penicillin and 500 mg ml−1 streptomycin (Gibco, #15140122). For the differentiation of cortical neurons the protocol described previously21 was followed with slight modifications. Briefly, hiPSC colonies were seeded…
How to choose parameters for kallisto single end mode?
How to choose parameters for kallisto single end mode? 1 Hello, I have some fastq files produced by NextSeq. The average fragment length is between 350-400bp. The library prep adds 139bp of adapters, so the inserts are 200-250bp. Would the kallisto command look like this? kallisto quant -i index -o…
Hospital Surveillance Sequencing Helps Link Cases to Nationwide Contaminated Eyedrop Outbreak
NEW YORK – A whole-genome sequencing (WGS)-based hospital outbreak surveillance program has helped researchers at the University of Pittsburgh to identify two drug-resistant Pseudomonas aeruginosa infections associated with a national outbreak of contaminated eyedrops. While the cases were ruled out as in-hospital transmissions, the findings illustrate the potential value of…
Shallow shotgun sequencing reduces technical variation in microbiome analysis
Participant selection and sample collection Informed consent was obtained for five adult volunteers. The study protocols were reviewed and approved by the Advarra Institutional Review Board (Advarra, Inc., Columbia, MD). All analyses were performed according to the relevant guidelines and regulations. Fecal collection was completed by self-sampling, which has proven…
Illumina TruSeq Stranded total Sample Preparation Protocol | CHMI services – TruSeq Stranded Total RNA
Preparation of total transcriptome libraries for sequencing on an Illumina dais Edit me Documentation TruSeq Running Absolute RNA Sample Prep Guide. This method makes a cDNA library of all RNA molecules presentational in your spot after rRNA depletion. Important: the succeed of this kit is dependent on of ability of…
MANAGEMENT’S DISCUSSION & ANALYSIS | MarketScreener
Our Management’s Discussion and Analysis (MD&A) will help readers understand our results of operations, financial condition, and cash flow. It is provided in addition to the accompanying condensed consolidated financial statements and notes. This MD&A is organized as follows: •Management’s Overview and Outlook. High level discussion of our operating results…
Illumina Sequencing Instruments Affected by Maximum Severity Vulnerability
Posted By HIPAA Journal on May 5, 2023 Healthcare providers and laboratory personnel have been warned about a maximum severity vulnerability in Illumina Universal Copy Service software used by its DNA sequencing instruments. The vulnerability affects Illumina products with Illumina Universal Copy Service (UCS) v2.x installed: iScan Controls Software (v4.0.0…
Vulnerabilities Discovered in Illumina DNA Sequencing Devices
Healthcare providers and laboratory personnel have been put on alert after two separate cybersecurity vulnerabilities were discovered in medical devices commonly used in clinical diagnostics and research.
Bioinformatics Analyst II job with Frederick National Laboratory
Bioinformatics Analyst II Job ID: req2894Employee Type: exempt full-timeDivision: Bioinformatics and Computational ScienceFacility: Frederick: ATRFLocation: 8560 Progress Dr, Frederick, MD 21701 USA The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The…
Illumina Software Raises Critical Warning for Medical Device Vulnerability
The Universal Copy Service (UCS) service in Illumina devices has been found to have critical security gaps that could allow attackers to execute code and take control of the devices, warns the US Cybersecurity and Infrastructure Security Agency (CISA). These devices are widely used worldwide, particularly for DNA sequencing. Attackers…
Illumina NGS instrument software vulnerable to cybersecurity breach: FDA
The U.S. Food and Drug Administration (FDA) last week warned healthcare providers and laboratory personnel about a cybersecurity vulnerability affecting software in Illumina instruments that may be specified either for clinical diagnostic use in sequencing a person’s DNA for various genetic conditions or for research use only (RUO). The sequencing…
Critical Vulnerabilities In Illumina Universal Copy Service Devices
1 US CISA warns of critical vulnerabilities affecting the security of Illumina devices. The vulnerabilities exist in the Illumina Universal Copy Service software, allowing remote code execution attacks. Illumina Universal Copy Service Vulnerabilities According to a recent CISA alert, at least two vulnerabilities were discovered in Illumina DNA sequencing devices….
FDA Warns of Cybersecurity Vulnerabilities in Certain DNA Sequencing Devices
Federal health officials are warning medical facilities that certain diagnostic DNA sequencing devices contain software vulnerabilities, which could make them susceptible to cybersecurity hacks.
FDA Warns Cybersecurity Vulnerability For Illumina Sequencers
The FDA issued a letter noting that nearly the entire Illumina Inc’s (NASDAQ: ILMN) sequencer lineup carries a cybersecurity vulnerability that could impact genomic data results or even result in a data breach. The agency said that the Universal Copy Service software in the Illumina NovaSeq 6000, NextSeq 500, NextSeq 550, NextSeq 550Dx NextSeq…
CISA, FDA warn of new Illumina DNA device vulnerability
Several U.S. agencies warned this week about a vulnerability affecting software in devices used for DNA research that would allow hackers access to sensitive patient information. The Food and Drug Administration (FDA) and the company behind the devices — Illumina — said they have not received any reports indicating the…
CISA Warns of Critical Flaws in Illumina’s DNA Sequencing Instruments
Apr 29, 2023Ravie LakshmananHealthcare / Cybersecurity The U.S. Cybersecurity and Infrastructure Security Agency (CISA) has released an Industrial Control Systems (ICS) medical advisory warning of a critical flaw impacting Illumina medical devices. The issues impact the Universal Copy Service (UCS) software in the Illumina MiSeqDx, NextSeq 550Dx, iScan, iSeq 100,…
Vulnerability in Illumina genome sequencing medical devices ranked 10.0
A critical vulnerability ranked 10.0 found in certain universal copy service software used in certain Illumina genome sequencing tools could enable a host of nefarious activities, including the remote upload and execution of code at the operating system level. The Cybersecurity and Infrastructure Security Agency (CISA) and the Food and…
FDA Roundup: April 28, 2023
For Immediate Release: April 28, 2023 Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA issued a final guidance for industry titled Smoking Cessation and Related Indications: Developing Nicotine Replacement Therapy Drug Products, which replaces the draft guidance…
Illumina Sequencers Face Cybersecurity Vulnerability, FDA Warns
NEW YORK – The US Food and Drug Administration said on Thursday afternoon that nearly the entire Illumina sequencer lineup carries a cybersecurity vulnerability that could impact genomic data results or even result in a data breach. In a letter to healthcare providers and laboratory personnel, the FDA said that…
Critical-rated security flaw in Illumina DNA sequencing tech exposes patient data
The U.S. government has sounded the alarm about a critical software vulnerability found in genomics giant Illumina’s DNA sequencing devices, which hackers can exploit to modify or steal patients’ sensitive medical data. In separate advisories released on Thursday, U.S. cybersecurity agency CISA and the U.S. Food and Drug Administration warned…
Vital-rated safety flaw in Illumina DNA sequencing tech exposes affected person information
The U.S. authorities has sounded the alarm a couple of essential software program vulnerability present in genomics large Illumina’s DNA sequencing gadgets, which hackers can exploit to change or steal sufferers’ delicate medical information. In separate advisories launched on Thursday, U.S. cybersecurity company CISA and the U.S. Meals and Drug…
FDA Issues Warning Regarding Cybersecurity Vulnerability in Illuminas Universal Copy Service Software
As of April 27, 2023, the U.S. Food and Drug Administration (FDA) has issued a warning regarding a cybersecurity vulnerability discovered in Illumina’s Universal Copy Service software. This vulnerability can potentially pose risks to patient health results and customer networks. Fortunately, the FDA has not received any reports indicating the…
Combining data from single- and paired-end sequencing done on same samples
Combining data from single- and paired-end sequencing done on same samples 0 Hi everyone, This is my first post in this community as I’m still fairly new to bioinformatics. Please forgive me if I make any mistakes. My current issue is in regards to reads of the same samples not…
Illumina gets cybersecurity warning from FDA over sequencing software
A cybersecurity vulnerability in Illumina DNA sequencing instruments could allow an unauthorized user to take control of the devices remotely or alter genomic data results, the U.S. Food and Drug Administration said Thursday in a warning to healthcare providers and laboratory personnel. The DNA-sequencing company first notified customers on April 5,…
Asia-Pacific and Middle East NGS Global Market to 2027:
Dublin, April 27, 2023 (GLOBE NEWSWIRE) — The “Asia-Pacific and Middle East NGS Market: Focus on Offering, Platform, Throughput, Technology Type, Application, End User, and Country Analysis – Analysis and Forecast, 2022-2027” report has been added to ResearchAndMarkets.com‘s offering. The Asia-Pacific and Middle East NGS market was valued at $1,055.6…
Illumina (ILMN) Q1 Earnings Beat Estimates, Margins Contract
Illumina Inc. ILMN reported adjusted earnings per share (EPS) of 8 cents in the first quarter of 2023, sailing past the Zacks Consensus Estimate of 2 cents by a remarkable margin. However, the bottom line declined 92.5% from the year-ago quarter’s earnings of $1.07. The adjustments exclude the impact of GRAIL…
Sequencing at Sea – Unlocking the Power of the Genome With eDNA and NextSeq(TM) 2000
FREE Breaking News Alerts from StreetInsider.com! StreetInsider.com Top Tickers, 4/24/2023 April 24, 2023 1:51 PM EDT Get inside Wall Street with StreetInsider Premium. Claim your 1-week free trial here. NORTHAMPTON, MA / ACCESSWIRE / April 24, 2023 / In 2022, Illumina and Minderoo Foundation announced a $40M AUD partnership to…
Sequencing at Sea – Unlocking the Power of the Genome With eDNA
April 24, 2023 – 1:45 pm NORTHAMPTON, MA / ACCESSWIRE / April 24, 2023 / In 2022, Illumina and Minderoo Foundation announced a $40M AUD partnership to leverage the power of genomics to accelerate scientific understanding of marine systems and help marine conservationists make informed decisions. The three-year partnership demonstrates…
DNA And Gene Chip Global Market Report 2023
New York, April 24, 2023 (GLOBE NEWSWIRE) — Reportlinker.com announces the release of the report “DNA And Gene Chip Global Market Report 2023” – www.reportlinker.com/p06451197/?utm_source=GNW , bioMérieux SA., Applied Microarrays Inc., Biometrix Technology Inc., Oxford Gene Technology, Affymetrix Inc., Bioneer Corp., and Eurofins Mwg Operon. The global DNA and gene…
Global MiRNA sequencing market is expected to register a revenue CAGR of 12% during the Forecast period 2032
Reports And Data The global Micro Ribonucleic Acid (MiRNA) sequencing assay market size is expected to register a revenue CAGR of 12% during the forecast period 2032. NEW YORK, NY, UNITED STATES, April 23, 2023 /EINPresswire.com/ — The Global MiRNA Sequencing Assay Market sequencing assays was valued at USD 594.16…
Illumina Urges Shareholders to Vote the WHITE Proxy Card FOR all Nine of Illumina’s Nominees
SAN DIEGO, April 20, 2023 /PRNewswire/ — Illumina, Inc. (NASDAQ: ILMN), a global leader in DNA sequencing and array-based technologies, today urged shareholders to vote in favor of Illumina’s slate of highly qualified director nominees. It also announced that its Annual Meeting will be held virtually on May 25, 2023, at…
Specific recognition of an FGFR2 fusion by tumor infiltrating lymphocytes from a patient with metastatic cholangiocarcinoma
Introduction Cholangiocarcinoma (CC) is a form of gastrointestinal cancer that originates from the epithelium of either intrahepatic or extrahepatic bile ducts. It accounts for approximately 3% of all gastrointestinal cancers, with reported incidence of one to two cases per 100,000 persons per year in the USA (and much higher incidence…
Illumina Instrument Type from fastq?
Illumina Instrument Type from fastq? 5 Hi, Any idea if there’s a way to get the Instrument type (i.e. NextSeq, HiSeq, etc), from the instrument name field in the Fastq read header? – I’ve tried looking for a map of sorts in Illumina’s documentation, but to no avail. Thanks, fastq…
Mutation-induced infections of phage-plasmids | Nature Communications
Media The minimal marine media, MBL media, was used for serial dilution growth of Tritonibacter mobilis A3R06. It contained 10 mM NH4Cl, 10 mM Na2HPO4, 1 mM Na2SO4, 50 mM HEPES buffer (pH 8.2), NaCl (20 g/liter), MgCl2*6H2O (3 g/l), CaCl2*2H2O (0.15 g/l), and KCl (0.5 g/l). Glucose was added as the only carbon source at a…
Bioinformatics Analyst II – Frederick National Laboratory
Bioinformatics Analyst II Job ID: req2894Employee Type: exempt full-timeDivision: Bioinformatics and Computational ScienceFacility: Frederick: ATRFLocation: 8560 Progress Dr, Frederick, MD 21701 USA The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The…
Liquid biopsy using cfDNA to predict radiation therapy response in solid tumors
Purpose: This study explored the potential feasibility of cell-free DNA (cfDNA) in monitoring treatment response through the measurement of chromosomal instabilities using I-scores in the context of radiation therapy (RT) for other solid tumors. Materials and methods: This study enrolled 23 patients treated with RT for lung, esophageal, and head…
Health Sciences genome sequencers a leap forward for research
Finding when and where DNA changes as a disease progresses allows for better treatment of chronic, genetic-based diseases including cancer, diabetes, and neurological and developmental disorders. At the University of Arizona, genome sequencers are used across multiple disciplines. But the newest genome sequencer in the UArizona Health Sciences offers the…
How to remove the contaminant reads from plants sequencing
How to remove the contaminant reads from plants sequencing 0 Hey guys. I want to assemble the genome of a plant species native to the Brazilian cerrado, which was sequenced by Illumina’s NextSeq (paired-end/short reads). However, even after quality control with the trimmomatic, the assemblers I used detected contaminants on…
Clinical Efficacy and Diagnostic Value of Metagenomic Next-Generation
Introduction Infections are the major cause of human deaths worldwide and present a rising threat to public security.1 Antimicrobial resistance is a major concern that is threatening our ability to treat bacterial infections.2 Delayed administration of antibiotics significantly increases the in-hospital mortality rate.3 The tragic outcome of infection highlights the…
How to demultiplex single-end dual indexed run
Hi all, I have data from a single-end run with a dual index structure generated by the NextSeq 500 instrument. I want to do the demultiplexing by bcl2fastq tool. How should my SampleSheet.csv structure and bcl2fastq script look like? I used aSampleSheet structure (shared below) with a bcl2fastq command (mentioned…
Multi-faceted metagenomic analysis of spacecraft associated surfaces reveal planetary protection relevant microbial composition
. 2023 Mar 22;18(3):e0282428. doi: 10.1371/journal.pone.0282428. eCollection 2023. Sarah K Highlander 1 , Jason M Wood 2 , John D Gillece 1 3 , Megan Folkerts 1 , Viacheslav Fofanov 3 4 , Tara Furstenau 3 , Nitin K Singh 2 , Lisa Guan 2 , Arman Seuylemezian 2 , James N Benardini 2 , David M Engelthaler …
Whole Exome Sequencing Market – Growth, Trends, COVID-19 Impact, And Forecasts (2023
ReportLinker The whole exome sequencing market is expected to register a CAGR of 22.1% over the forecast period. The outbreak of the COVID-19 pandemic pushed the pharmaceutical industry into action, with a race to develop therapeutic and preventive interventions. New York, March 20, 2023 (GLOBE NEWSWIRE) — Reportlinker.com announces the…
High-quality single amplicon sequencing method for illumina MiSeq platform using pool of ‘N’ (0-10) spacer-linked target specific primers without PhiX spike-in
Background: Illumina sequencing platform requires base diversity in the initial 11 cycles for efficient cluster identification and colour matrix estimation. This limitation yields low-quality data for amplicon libraries having homogeneous base composition. Spike-in of PhiX library ensures base diversity but reduces the overall number of sequencing reads for data analysis….
Cambridge: City of Innovation – The ‘beer summit’ that generated a genomic revolution
When you hear Next Generation Sequencing (NGS), you think Illumina Inc. Illumina is widely regarded as the giant of NGS, with an estimated 80% share of the global gene sequencing market. At the heart of Illumina’s nucleic acid sequencing technologies is sequencing-by-synthesis (SBS), a chemistry technology with a humble and…
How to demultiplex single end – dual index run
Hi all, I have data from a single-end run with a dual index structure generated by the NextSeq 500 instrument. I want to do the demultiplexing by bcl2fastq tool. How should my SampleSheet.csv structure and bcl2fastq script look like? I used aSampleSheet structure (shared below) with a bcl2fastq command (mentioned…
Illumina Underscores Commitment to Shareholder Value and Responds to Carl Icahn’s Statements
Illumina’s plan will maximize shareholder value Illumina is engaged with regulators to define GRAIL’s path forward as expeditiously as possible Icahn’s director nominees do not add value to the Board and will damage Illumina’s core business SAN DIEGO, March 20, 2023 /PRNewswire/ — Illumina (NASDAQ: ILMN), a global leader in…
Whole Exome Sequencing Market – Growth, Trends, COVID-19
New York, March 20, 2023 (GLOBE NEWSWIRE) — Reportlinker.com announces the release of the report “Whole Exome Sequencing Market – Growth, Trends, COVID-19 Impact, And Forecasts (2023 – 2028)” – www.reportlinker.com/p06431219/?utm_source=GNW The whole exome sequencing market is expected to register a CAGR of 22.1% over the forecast period. The outbreak…
Targeted DNA sequencing of high-grade serous ovarian cancer (HGSC) tumour and normal samples from 15 patients with homologous recombination deficiencies. The dataset includes fastq files from 243 HGSC tumours (15 primary, 3 relapse, 225 end-stage) and 15 normals from 15 HGSC patients. Following target hybrid capture of 63 genes involved in DNA repair and response to treatment with an Agilent SureSelect XT panel, sequencing libraries were generated using the SureSelect XT Low Input Target Enrichment System (Agilent) as per the manufacturer’s protocol. Libraries were sequenced on an Illumina NextSeq 500 at the Peter MacCallum Cancer Centre (Melbourne, Australia).
Dataset Description Targeted DNA sequencing of high-grade serous ovarian cancer (HGSC) tumour and normal samples from 15 patients with homologous recombination deficiencies. The dataset includes fastq files from 243 HGSC tumours (15 primary, 3 relapse, 225 end-stage) and 15 normals from 15 HGSC patients.Following target hybrid capture of 63 genes…
Cancer Biopsy Market accounting for a CAGR of nearly 19% from 2023 to 2033
PRESS RELEASE Published March 9, 2023 The Cancer Biopsy market revenues were estimated at US$ 22.2 Bn in 2022 and is anticipated to grow at a CAGR of 18% from 2023-2033, according to a recently published Future Market Insights report. By the end of 2033, the market is expected to reach US$ 131.4 Bn. The…
Early Post Doctoral Researcher – Kenya
JOB PURPOSE: We are seeking Early Post – Doctoral Researcher for a three-year WELLCOME funded G2P – Global Knowledge Exchange to Enable In Country Risk Assessment of SARS CoV-2 Variants aimed at determining the zoonotic potential of SARS-CoV-2 variants. The candidate will work with a team to develop system serology…
Sample Requirements | Source BioScience
Below is listed the optimal sample requirements needed. The stated volumes provide us with enough of the sample for our internal sample checks and library preparation. Samples can be provided more concentrated than suggested and will be diluted as needed. Please contact your Sales representative for minimum sample requirements. …
Sequencer (Illumina MiSeq) | Editable Science Icons from BioRender
Use this icon in BioRender along with 1000s of others to make your next science figure in minutes SIGN UP FREE [{“image”:”res.cloudinary.com/dlcjuc3ej/image/upload/v1561473348/ebbn9qyuttq9yjor15pm.svg#/keystone/api/icons/5d12314684fc6c04006a9878/sequencer-illumina-miseq.svg”,”waterMarkImage”:”icons.biorender.com/w550xh620/5d12314684fc6c04006a9878/sequencer-illumina-miseq.png”},{“image”:”res.cloudinary.com/dlcjuc3ej/image/upload/v1561473348/xhihfjtej5g1stsxuskc.svg#/keystone/api/icons/5d12314684fc6c04006a9877/sequencer-illumina-miseq.svg”,”waterMarkImage”:”icons.biorender.com/w550xh620/5d12314684fc6c04006a9877/sequencer-illumina-miseq.png”},{“image”:”res.cloudinary.com/dlcjuc3ej/image/upload/v1573575912/a12usyeepidrrrsqosfd.svg#/keystone/api/icons/5dcadcea775675000410407c/sequencer-illumina-miseq.svg”,”waterMarkImage”:”icons.biorender.com/w550xh620/5dcadcea775675000410407c/sequencer-illumina-miseq.png”}] Keywords lab,lab equipment,equipment,technology,sequencer,sequencing,illumina,next-generation sequencing platform,sequencing platform,NGS,NextSeq,iSeq,DNA sequencer,RNA sequencer,RNA seq,DNA seq Read more here: Source link
bcl2fastq was killed with signal -11
cellranger-arc mkfastq Error: bcl2fastq was killed with signal -11 0 Hi all, I’m attempting to use cellranger-arc mkfastq to convert BCL files to FASTQ files, but encountered with errors and would like help from you. Command I ran is: cellranger-arc mkfastq –id=ATAC1_fastq \ > –run=/mnt/c/Users/helen/Desktop/Analysis/Raw_bcl_files/ATAC1/230120_NB551308_0209_AH5W5LBGXN \ > –csv=/mnt/c/Users/helen/Desktop/Analysis/230120_NB551308_0209_AH5W5LBGXN.csv \ >…
Innovative technologies crowd the short-read sequencing market
There’s an old saying in the field of technology: “Nobody ever got fired for buying IBM” — a reference to the company’s once-ubiquitous computers. Replace IBM with Illumina, a biotechnology company in San Diego, California, and the same could be said of DNA sequencing today. Keith Robison, a computational biologist…
From 2023 through 2033, Cancer Biopsy sales to expand at a CAGR of over 18%, Reveals Future Market Insights
The Cancer Biopsy market revenues were estimated at US$ 22.2 Bn in 2022 and is anticipated to grow at a CAGR of 18% from 2023-2033, according to a recently published Future Market Insights report. By the end of 2033, the market is expected to reach US$ 131.4 Bn. The…
AGBT: Illumina Offers First Look Under the Hood for Complete Long Reads Product
HOLLYWOOD, Florida – Illumina provided the first explanation for how its new Complete Long Reads (CLR) product will work as well as some customer data and testimonials at a Wednesday workshop here at the Advances in Genome Biology and Technology annual meeting. First, DNA molecules are tagmented to generate long…
New genome sequencer at UA Steele Children’s Center to help researchers improve patient outcomes
The People Acting Now Discover Answers Core for Genomics and Microbiome Research at the University of Arizona Steele Children’s Research Center is using its new best-in-class genome sequencing machine to analyze genomes with more accuracy and speed than was previously possible. The PANDA Core is an arm of the Steele…
calctruequality in bbmap
calctruequality in bbmap 1 I’m trying to recalibrate Q scores of a NextSeq run using MiSeq contigs assembled with Tadpole. The commands I used to map the reads to the reference were as follows: bbmap.sh in=concatABC.fastq.gz outm=mapped.sam ref=./Lpe09_06TdpAssemblies/contigs09_06.fa ignorequality maxindel=100 minratio=0.4 ambig=toss qahist=qahist_raw.txt qhist=qhist_raw.txt mhist=mhist_raw.txt The command I used to…
Spatial and NGS Dominate Proceedings at AGBT 2022
Attending the Advances in Genome Biology and Technology (AGBT) meeting in June 2022 in Orlando, FL, was like drinking from a firehose of genomic information. Or rather, two firehoses. The first let loose a steady stream of information about progress in spatial biology. Speakers shared their excitement over new discoveries,…
Illumina, Pacific Biosciences, And Oxford Nanopore Market Position Comparison
piola666/E+ via Getty Images Investment Thesis Gene sequencing revolutionized our understanding of the human genome and its function. Today, we can accurately identify thousands of genetic variations that contribute to human health and disease, opening up the possibility of personalized medicine – creating medicine that is customized to the individual….
biological vs. technical definition of “insert size”
biological vs. technical definition of “insert size” 0 I’m trying to simulate metagenomic reads using Grinder. I want to simulate paired-end reads, so I need to select arguments for insert size and distribution. This is what they say: -id <insert_dist>… | -insert_dist <insert_dist>… Create paired-end or mate-pair reads spanning the…
Next Generation Sequencing Market Business Strategies,
Next Generation Sequencing Market The Business Research Company’s global market reports are now updated with the latest market sizing information for the year 2023 and forecasted to 2032 As per the next-generation sequencing market report by The Business Research Company, the growing number of cases with chronic conditions such as…
Whole Genome DNA Illumina sequencing – Infravec2
Description Material provided: dataUnit definition: Whole Genome SequencingLibrary Preparation: Illumina DNA Prep or TruSeq Nano Sample Prep Kit400 million reads for 2×150 Paired End Length equivalent to ca 30X sequence depth for 1 sample of Aedes spp (estimated genome size: 1.38 Gb) or to ca 100X sequence depth for 1…
Multi-pathogenic pneumonia in HIV-infected patients
Introduction Pulmonary infection is the most common cause of morbidity and mortality in immunocompromised patients.1 The pathogens spectrum of pneumonia that can affect patients with human immunodeficiency virus (HIV) is wide, such as bacterial, fungal, viral, parasitic organisms, and so on.2–4 Compared to patients with monomicrobial pulmonary infection, the clinical…
Genetic determinants and absence of breast cancer in Xavante Indians in Sangradouro Reserve, Brazil
Ethics statement Authorization from Fundação Nacional do Índio (FUNAI) was acquired after approval from the Research Ethics Committee of the Faculty of Medicine in the Federal University of Mato Grosso (UFMT), and the National Commission of Research Ethics (authorization #1004/2001). Written consents, which were recorded and archived, were acquired from…
Nextseq and Miseq data output difference?
Nextseq and Miseq data output difference? 2 Hi, Is it ok to run a Mixcr pipeline on a TCR sequencing dataset, half of which was processed on Nextseq and half on Miseq? What is the major difference among Nextseq and Miseq platforms? Thanks, Payal sequencing • 2.0k views • link…
Broad Institute Study Evaluates Ultima Genomics Sequencer for Single-Cell RNA-Seq
NEW YORK – Results from single-cell RNA sequencing libraries run on the new Ultima Genomics UG100 are “very similar” to those produced on Illumina’s NovaSeq, a new study says. However, the platform shows bias against 3′ gene expression libraries. Led by researchers from the Broad Institute as part of a…
Bronchoalveolar Lavage Fluid for Metagenomic Sequencing
Introduction Severe pneumonia is one of the most common causes of infectious diseases among patients in the intensive care unit (ICU), and this can lead to various complications and high mortality.1–3 Timely and accurate pathogen diagnoses are crucial for appropriate antimicrobial therapy and improved clinical outcomes. However, the low detection…
Targeted inhibition of ubiquitin signaling reverses metabolic reprogramming and suppresses glioblastoma growth
Cell culture Human glioblastoma cells (U87MG and U87MG-Luc) and human embryonic kidney cells (HEK293) were obtained from the American Type Culture Collection (Manassas, Va.). Cells were cultured in Dulbecco’s Modified Eagle Medium supplemented with 10% fetal bovine serum (Gibco™ Fetal Bovine Serum South America, Thermo Scientific Fisher-US), 2 mM l-glutamine, 50 U/ml…
How many lanes does the Nextseq (illumina) flow cell have?
How many lanes does the Nextseq (illumina) flow cell have? 1 Hi all, How many lanes does the Nextseq (illumina) flow cell have? Thanks. sequencing • 12k views MiSeq – 1 lane cells HiSeg machines had 8 lanes in High Output Mode and 2 lane cells in Rapid Mode (only…
CISA Warned About Critical Vulnerabilities in Illumina’s DNA Sequencing Devices
The U.S. Cybersecurity and Infrastructure Security Agency (CISA) and Food and Drug Administration (FDA) have issued an advisory about critical security vulnerabilities in Illumina’s next-generation sequencing (NGS) software. Three of the flaws are rated 10 out of 10 for severity on the Common Vulnerability Scoring System (CVSS), with two others…
Trimming adaptors and primers for RNAseq reads
Trimming adaptors and primers for RNAseq reads 2 Hi all, I have RNA sequencing (sequenced on NextSeq 2000) reads that I know I need to cut the adaptor sequences off of and was planning to use cutadapt to do so. I have identified the adaptor sequence in my reads, but…
illumina miseq reagent Bids, RFP & Government Contracts
Reagent (Chemistry) Kits Quick View Type : Bid Notification Due : 04 Aug, 2017 (about 4 years ago) Posted : about 4 years ago Started : 28 Jul, 2017 (about 4 years ago) All of which require Reagent (Chemistry) Kits for data analysis as follows:• Sequencing by Synthesis (SBS) Kits•…
Pollinator sharing, copollination, and speciation by host shifting among six closely related dioecious fig species
Sampling Six dioecious fig species (F. erecta, F. formosana, F. vaccinioides, F. abelii, F. pyriformis, and F. variolosa) and their pollinator wasp species were examined in this study. As mentioned in the Introduction, these fig species were considered to be well suited for this study because they are distributed in…
Low transcript quantification with Salmon using GRCm39 annotations
Hi everyone, first time working with mouse samples and unfortunately, there are fewer resources available for the latest mouse Ensembl genome than I was expecting. What I’ve done: I performed rRNA depletion on total RNA extracted from mouse tissue and created Illumina libraries using a cDNA synthesis kit with random…
Transcriptional kinetics and molecular functions of long noncoding RNAs
Ethical compliance The research carried out in this study has been approved by the Swedish Board of Agriculture, Jordbruksverket: N343/12. Cell culture Mouse primary fibroblasts were derived from adult (>10 weeks old) CAST/EiJ × C57BL/6J or C57BL/6J × CAST/EiJ mice by skinning, mincing and culturing tail explants (for at least 10 d) in DMEM high…
Extracellular circulating miRNAs as stress-related signature to search and rescue dogs
Study approval was provided by the Research Ethics Committee of the University of Perugia (report n.2018-21 of 11/12/2018) according to Italian Ministry of Health legislation18. All methods were carried out following relevant guidelines and regulations and the study was carried out in compliance with the ARRIVE guidelines. Informed consent is…
QuantSeq 3’ mRNA-Seq Library prep kits: Lexogen
QuantSeq 3’ mRNA-Seq Library Prep kits from Lexogen offers cost-efficient analysis of differential gene expression via 3’ mRNA-seq library preparation. Requiring fewer reads per samples and capable of multiplexing a high number of samples on a single sequencing lane, the 3’ mRNA-Seq technology simplifies your gene expression projects with no…
Phylogenomic analysis of CTX-M-15-producing Enterobacter hormaechei belonging to the high-risk ST78 from animal infection: Another successful One Health clone?
Available online 18 February 2022 doi.org/10.1016/j.jgar.2022.02.010Get rights and content Highlights • ESBL-positive Enterobacter cloacae complex members are critical priority pathogens. • E. hormaechei belonging to sequence type (ST) ST78 is an emergent high-risk clone. • Phylogenomic data of an E. hormaechei ST78/CTX-M-15 infecting a calf is presented. • E. hormaechei…
Single-cell delineation of lineage and genetic identity in the mouse brain
STICR lentiviral library preparation and validation We synthesized a high-complexity lentivirus barcode library that encodes approximately 60–70 million distinct oligonucleotide RNA sequences (STICR barcodes). STICR barcodes comprised three distinct oligonucleotide fragments cloned sequentially into a multicloning site within the 3′ UTR of an enhanced green fluorescent protein (eGFP) transgene under…
Bacterial endosymbionts protect beneficial soil fungus from nematode attack
A healthy soil nourishes plants and animals, purifies water and air, and promotes sustainable agriculture. Characteristic for highly complex and competitive soil ecosystems are the frequent and direct interactions between all soil-dwelling microorganisms, animals, and plants (1, 2), all of which need to be provided with minerals and carbon sources….
NextSeq 2000 Sequencing | University of Minnesota Genomics Center
The NextSeq 2000 is Illumina’s newest platform that uses advancements in optics, instrument design, and 2-channel chemistry to increase output. This new sequencing technology makes it possible for researchers to sequence a range of conventional and emerging applications by increasing throughput while cutting down on costs per run when compared…
Gene mutation analysis in papillary thyroid carcinoma
Introduction Thyroid tumors are the most common malignant tumors of the endocrine system, and their incidence has been increasing in the recent decades. Currently, there are some target drugs that can effectively treat PTC, and next-generation sequencing (NGS) can be used for targeted therapy. In order to make better informed…