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Search results for indels
indels
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20 search results found
Manta
⭐
333
Structural variant and indel caller for mapped sequencing data
Svaba
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211
Structural variation and indel detection by local assembly
Strelka
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204
Strelka2 germline and somatic small variant caller
Lancet
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145
Microassembly based somatic variant caller for NGS data
Sigminer
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119
🌲 An easy-to-use and scalable toolkit for genomic alteration signature (a.k.a. mutational signature) analysis and visualization in R https://shixiangwang.github.io/sigminer/reference/
Tracy
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92
Basecalling, alignment, assembly and deconvolution of Sanger Chromatogram trace files
Abra2
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69
ABRA2
Bayestyper
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52
A method for variant graph genotyping based on exact alignment of k-mers
Gvanno
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43
Generic human DNA variant annotation pipeline
Platinumgenomes
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42
The Platinum Genomes Truthset
Clairs
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42
ClairS - a deep-learning method for long-read somatic small variant calling
Indigo
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29
Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products
16gt
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26
Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model
Gssplayground
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21
Lightweight single-html-file-based Genome Segments playground for Visualize genome features cluster(gene arrow map or other features), add synteny among genome fragments or add crosslink among features, add short(PE/MP)/long reads(pacbio or nanopore) mapping or snpindel in vcf(not support complex sv yet), support all CIGAR of sam alignment, directly modify almost all features in Chrome by click the feature
Homoplasyfinder
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12
A tool to identify and annotate homoplasies on a phylogeny and sequence alignment
Indelpost
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11
Python library for simple and complex indels.
Metagwastoolkit
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10
A ToolKit to perform a Meta-analysis of Genome-Wide Association Studies
Bioinformatics
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10
A suite of bioinformatics data processing and analysis pipelines, software, and training resources for common DNA and RNA sequence analysis methods.
Dockstore Cgpwgs
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9
Dockstore implementation of CGP core WGS analysis
Crispr_dart
⭐
7
A workflow to analyse sequence mutations in CRISPR-CAS9 targeted amplicon sequencing data
Related Searches
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Indels Snv (10)
Bioinformatics Indels (9)
Sequencing Indels (6)
Vcf Indels (6)
Somatic Variants Indels (6)
Snps Indels (6)
C Plus Plus Indels (5)
1-20 of 20 search results
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