WebNov 18, 2024 · align paired end FASTQ files to contigs.fasta file with minimap2 to get SAM file. convert SAM to BAM with samtools. sort and index BAM file. load BAM file into IGV and load contigs.fasta as the reference. In the IGV GUI, I have colored alignments by insert size and pair orientation. This has revealed a bunch of insertions, tandem duplications ... WebHi all, Then you'll want to do a fastq_to_fasta : http://hannonlab.cshl.edu/fastx_toolkit/commandline.html#fastx_manipulation_example James W. MacDonald wrote: > Hi ...
samtools-fqidx(1) manual page
WebJul 4, 2013 · I can convert my SAM to a BAM with samtools view -Sbh, but after bwa aln, the next step, bwa samse, still requires raw FASTQs as one of the inputs. Picard … Webbamtofastq - convert SAM, BAM or CRAM files to FastQ SYNOPSIS bamtofastq [options] DESCRIPTION bamtofastq reads a SAM, BAM or CRAM file from standard input and converts it to the FastQ format. The output can be split into multiple files according to the pair flags of the reads involved. chocolate icing recipe with marshmallows
how can I convert Fastq to SAM file? ResearchGate
WebWe can output to BAM instead and convert (below), or modify the SAM @SQ header to include MD5 sums in the M5: field. samtools sort -O bam -T /tmp -l 0 -o yeast.bam yeast.sam. The “-l 0” indicates to use no compression in the BAM file, as it is transitory and will be replaced by CRAM soon. WebWe will use samtools to view the sam/bam files. Let’s take a look at the first few lines of the original file. We’ll use the samtools view command to view the sam file, and pipe the output to head -5 to show us only the ‘head’ of the file (in this case, the first 5 lines). samtools view aligned_reads.sam head -5. Output: WebSamtools can be used to convert between sam and bam:-b indicates that the input file will be in BAM format-S indicates that the stdout should be in SAM format; samtools view … gray and green floor tile