WebNov 16, 2024 · 14 samtools merge merged.bam *.bam is efficient enough since the input files are sorted. You can get a bit faster with sambamba and/or biobambam, but they're not typically already installed and IO quickly becomes a bottleneck anyway. Share Improve this answer Follow answered May 19, 2024 at 7:06 Devon Ryan 19.4k 2 27 58 WebNov 19, 2024 · The first is a BAM file containing the raw full-length passes of the sequencing which includes subreads, errors, primers, and the smart bell sequence. The …
MultiQC - fastQC summary tool - University of Texas at Austin
Webfastq to final valid pairs bam file - step by step ¶ Alignment ¶ Now that you have a genome file, index file and a reference fasta file you are all set to align your Micro-C library to the reference. Please note the specific settings that are needed to map mates independently and for optimal results with our proximity library reads. WebNov 24, 2024 · 1 Answer Sorted by: 4 A BAM file should have a roughly similar size to a compressed FASTQ file, because they're both compressed files that contain similar information. BAM will be slightly larger, because it contains information about mapping and differences from the reference. phlebotomy competency test
From fastq to final valid pairs bam file — Micro-C 0.1 …
WebJan 8, 2024 · I have a list of samples going through Snakemake. When I arrive at my fastqc step, I suddenly have two files per sample (an R1 and R2 file). Consider the following rule: WebDNA-Seq-Analysis The shell script for samplesheet.csv is present in shell_wes.sh saved as ./steps_shell_wes.sh Step 1: Quality Control Step 2: Trimming Step 3: Mapping Step 4: Processing SAM/BAM files Step 5: Removing duplicates Step 6: Variant Calling Step 7: Variant Filtering Step 8: Annotation Webfastq to final valid pairs bam file - step by step ¶ Alignment ¶ Now that you have a genome file, index file and a reference fasta file you are all set to align your Micro-C library to the … phlebotomy competency