WebNov 10, 2024 · Description. Download SamTools 0.9.41 from our website for free. The default filename for the program's installer is SAMTOOLS.EXE. This free program is an … WebJun 8, 2024 · cat GRCh38.karyo.bed awk ' {print $3}' datamash sum 1 3088286401 I would like to know how to run samtools depth so that it produces 3,088,286,401 entries when run against a GRCh38 bam file: samtools depth -b $bedfile -a $inputfile I tried it for a few bam files that were aligned the same way, and I get differing number of entries:
Ubuntu Manpage: samtools cat - concatenate files together
WebOct 2, 2024 · samtools cat would get a lot slower if you want to do a full merge, but it might be possible to preserve its speed in simpler cases. In the most complicated case, it would … Websamtools-cat (1) Bioinformatics tools samtools-cat (1) NAME samtools cat - concatenate files together SYNOPSIS samtools cat [ -b list ] [ -h header.sam ] [ -o out.bam] in1.bam in2.bam [ ... ] DESCRIPTION Concatenate BAMs or CRAMs. Although this works on either BAM or CRAM, all input files must be the same format as each other. richard slusser obituary
samtools - Online in the Cloud
WebFeb 10, 2024 · Samtools sort: most efficient approach to sort a single sample after aligning split .fastq files. Related to my other question ( Samtools sort: most efficient memory and … Web(#1333; fixed #1332) * Fixed a bug in samtools cat, which prevented the command from running in multi-threaded mode. Thanks to Alex Leonard for reporting the issue. (#1337; fixed #1336) * A couple of invalid CIGAR strings have been corrected in the test data. (#1343) * The documentation for `samtools depth -s` has been improved. WebSep 26, 2024 · This cat code should concatenate all files it finds matching the input ({}) from uniq in the directory in which the code is run. It will call the output file: 102697-001-001_R1.fastq.gz. I know that it doesn't automatically capture the R1. Perhaps someone could suggest a way to capture R1 in my code? richard slye