#
samtools
Here are 73 public repositories matching this topic...
The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
bioinformatics
modern
cpp17
fasta
blast
seqan
fastq
samtools
sequence-alignment
fm-index
sequence-analysis
cpp20
cpp-concepts
-
Updated
May 23, 2022 - C++
WebAssembly modules for genomics
javascript
bioinformatics
genomics
webassembly
wasm
awk
jq
gawk
htslib
bedtools
samtools
bcftools
bowtie2
minimap2
bhtsne
seqtk
wgsim
modbam2bed
seq-align
kalign
-
Updated
May 20, 2022 - Shell
Multi-sample somatic variant caller
docker
bam-files
pipeline
nextflow
ngs
regression
variants
somatic-mutations
samtools
negative-binomial-regression
-
Updated
Jan 27, 2022 - R
-
Updated
Mar 7, 2021 - Forth
Genopo a.k.a. F5N - A nanopore sequencing analysis toolkit for Android smartphones https://nanoporetech.com
android
toolkit
bioinformatics-pipeline
samtools
sequence-alignment
minimap2
nanopolish
mobile-genomics
portable-genomics
-
Updated
Aug 2, 2021 - Java
The ChIP-Seq peak calling algorithm using convolution neural networks
bioinformatics
tensorflow
gpu
docker-image
chip-seq
atac-seq
nvidia-docker
convolutional-neural-network
samtools
cnn-model
ngs-analysis
peak-calling
progressbar2
-
Updated
Jan 18, 2021 - Python
RNAseq pipeline for alternative splicing junctions
-
Updated
Jan 21, 2022 - R
Collecting Genotypes from ENA and make their SNPs
-
Updated
Sep 27, 2021 - Python
Analysis pipeline for processing paired-end Illumina reads obtained after ancient mtDNA target enrichment capture.
-
Updated
Mar 27, 2020 - Shell
CREST-seq peak calling.
-
Updated
Jun 26, 2017 - C++
Small test to compare AWS and HPC on a very simple workflow
-
Updated
Mar 15, 2018 - Shell
-
Updated
Jul 30, 2020 - Python
rna-seq
deseq2
star
samtools
featurecounts
bowtie2
cutadapt
fastqc
rna-seq-pipeline
htseq-count
tophat2
-
Updated
Dec 27, 2019 - Jupyter Notebook
Take information about snps on short sequence reads and accurately place the snps in a reference genome
-
Updated
Jun 26, 2020 - Python
fxtools: light-weight processing tool for FASTA/FASTQ/BAM format data
-
Updated
Apr 7, 2022 - C
Hilbert Mapper is a C++ implementation of Hilbert's space filling curve to represent read coverage on genomic sequences. Although it can be used to represent any unidimensional vector of positive numerical data.
-
Updated
Oct 23, 2018 - C++
A nodejs-based service for requests for tabix-indexed genomic data
-
Updated
Nov 12, 2019 - JavaScript
Improve this page
Add a description, image, and links to the samtools topic page so that developers can more easily learn about it.
Add this topic to your repo
To associate your repository with the samtools topic, visit your repo's landing page and select "manage topics."
When working with very large SAM files it is often convenient to remove sequence and quality information to reduce storage and improve I/O.
Following from this it would be convenient to have a
stripSeqQualfunction that replaces the two fields with*.