Tag: bowtie2-align
Error, fewer reads in file specified with -1 than in file specified with -2
Bowtie2: Error, fewer reads in file specified with -1 than in file specified with -2 1 Hi all, This is my first time attempting to align sequences to a reference index. I am using bowtie2 with the -1 and -2 arguments and have gotten the following error message: Error, fewer…
“bowtie2 died with signal 9 (KILL)” error message, having trouble figuring out how to fix my script
Hello! I am working on assembling a transcriptome of the terminal ganglion of the cricket (Gryllus bimaculatus). We are working on a non-model species and thus did not remove ribosomal contamination during library prep. We want to remove ribosomal contamination bioinformatically, and I am mapping our sequences, which have been…
Bowtie Parameter Switch Error
Bowtie Parameter Switch Error 1 I’m having this problem when running bowtie2 and can not figure it out. I am running a fairly basic bowtie2 command shown here bowtie2 –very-sensitive -x /usr/lusers/achits/achits/genomes/Xtropicalis9/Xtropicalis9 -1 z1.fastq -2 z2.fastq -X 2000 -p 14 -S and for some reason the error I’m getting is…
trying to look the version of the programs under miniconda3 directory
trying to look the version of the programs under miniconda3 directory 0 Hello, I had to uninstall miniconda3 on my previous HPC. The point is that I made a backup of the miniconda3 directory where all my programs and environments are. Is there a way to see the version of…
(ERR): bowtie2-align exited with value 13
bowtie2 – (ERR): bowtie2-align exited with value 13 1 I am trying to run bowtie2. but following error are occuring everytime bowtie2 –very-fast-local -x bowtie -q -1 R1.fastq -2 R2.fastq -s aligned.sam Saw ASCII character 10 but expected 33-based Phred qual. terminate called after throwing an instance of ‘int’ Aborted…
Use RSEM and Bowtie2 to align paired-end sequences
Use RSEM and Bowtie2 to align paired-end sequences 0 I want to use rsem-calculate-expression and bowtie2 aligner to align paired-end sequence based on the following conditions: 2 processors generate BAM file very fast bowtie2 sensitivity append gene/transcript name My code: rsem-refseq-extract-primary-assembly GCF_000001405.31_GRCh38.p5_genomic.fna GCF_000001405.31_GRCh38.p5_genomic.primary_assembly.fna rsem-prepare-reference –gff3 GCF_000001405.31_GRCh38.p5_genomic.gff –bowtie2 –bowtie2-path /bowtie2-2.4.5-py39hd2f7db1_2 –trusted-sources…
error while loading shared libraries
Question: Question: bowtie2-align-s: error while loading shared libraries Abhinav26 days ago Question: bowtie2-align-s: error while loading shared libraries /home/emilyw/.conda/envs/shotgun_134/bin/bowtie2-align-s: error while loading shared libraries: libtbb.so.2: cannot open shared object file: No such file or directory (ERR): Description of arguments failed! Exiting…
Issue with fastq after converting phred 64 to phred 33 quality scores
Hello, I ran seqtk seq -VQ64 read1.fastq.gz > read1_phred33.fastq to convert my 64 based phred score reads to 33 based phred score phred reads. However when I attempted to run them through tophat alignment I got this error: Saw ASCII character 4 but expected 33-based Phred qual. terminate called after…
Weird error from BWA and BOWTIE2
Weird error from BWA and BOWTIE2 1 Hi community, Recently I have used BWA and Bowtie2 to align simulated DNA sequencing data to test our sequencing simulator. I got some errors from both aligners: BWA: submit.sh: line 48: 6881 Segmentation fault (core dumped) BOWTIE2: terminate called after throwing an instance…
bowtie2-align died with signal 24 (XCPU) (core dumped)
(ERR): bowtie2-align died with signal 24 (XCPU) (core dumped) 0 Hi all, it is my first time using bowtie2, and I have a problem. I conducted the following command for reads mapping: bowtie2 -q –local -x mm10 -U SRR5839956_trimmed.fq -S SRR5839956.sam It created a 600MB sam file then come with…