There are 1 repository under bam-files topic.
Learning the Sequence Alignment/Map format
AltAnalyze is a multi-functional and easy-to-use software package for automated single-cell and bulk gene and splicing analyses. Easy-to-use precompiled graphical user-interface versions available from our website.
Sequence alignment tools
Multi-sample somatic variant caller
:vertical_traffic_light: Run Picard on BAM files and collate 90 metrics into one file.
Splice junction analysis and filtering from BAM files
create a interactive coverage plot dashboard from bam files and add gb, vcf and bed tracks
knowledge-based genotyping of cancer hotspots from the tumor BAM files
Split a BAM file by haplotype support
Utilities for analyzing next generation sequencing data.
Datastores for reads, not your papa's FASTQ files.
Collection of simple C scripts for parsing vcf or bam files using the htslib C library. These scripts can be used as the starting point for more complex scripts
A command line tool (in Kotlin/JVM) for intuitively visualizing BAM alignments. (Currently unmaintained)
Analysis pipeline for processing paired-end Illumina reads obtained after ancient mtDNA target enrichment capture.
The DKFZ alignment workflow plugin originally developed at the eilslabs
A Python3 script to quickly spot check 10 random sequences from a BAM/FASTx file.
Udo Stenzel's biohazard-tools — a collection of command-line utilities for bioinformatics [MIRROR]
A python package storing different tools for different NGS operations
Genomic data manipulation tool
Nextflow-based BAM-to-FASTQ conversion and FASTQ-sorting workflow.
Apply samtools addreplacerg to add a new read group and assign all reads to it in a BAM file