The program annotates low-coverage regions of sequences in fasta format
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Updated
Dec 18, 2023 - Python
The program annotates low-coverage regions of sequences in fasta format
Detect single-cell technology that was used to generate a set of FASTQ files or a single BAM file.
Проект: Место
Snakemake workflow to generate BAM alignment statistics on the BIH cluster.
Udo Stenzel's perl-ngs — a collection of Perl tools for next-generation sequencing [MIRROR]
SAMtools and BCFtools (v1.10) for manipulating next-generation sequencing data, from bioconda
Produce a report on a BAM file listing useful information
Commodore 64 disk image utility
Tool for adding genomic variants to an existing genome (in SAM/BAM/CRAM format). Currently supported variants are SNVs, indels and SVs (insertions, deletions, translocations, inversions and duplications). It generates realistic genomes as almost always less than 99% of the original real genome is modified.
Data dictionary and procedures for the Body Advocacy Movement Study (2020-). https://embark-lab.github.io/BAM-codebook/
Generalized Additive Forecasting Mortality
A collection of user scripts and Tool Labs tools intended for users of Wikimedia Foundation wikis.
Udo Stenzel’s jivebunny — a probabilistic demultiplexer for Illumina sequencing data [MIRROR]
Add a description, image, and links to the bam topic page so that developers can more easily learn about it.
To associate your repository with the bam topic, visit your repo's landing page and select "manage topics."