-
-
-
pepper Public
Forked from kishwarshafin/pepperPEPPER-Margin-DeepVariant
Python MIT License UpdatedJul 8, 2022 -
igv Public
Forked from igvteam/igvIntegrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
-
pbRUGD-workflow Public
Workflow for the comprehensive detection and prioritization of variants in human genomes with PacBio HiFi reads
-
hts-specs Public
Forked from samtools/hts-specsSpecifications of SAM/BAM and related high-throughput sequencing file formats
TeX UpdatedDec 3, 2020 -
pbRUGD-www Public
Web browser-based system to evaluate variant calls in human genomes from PacBio HiFi reads
-
vim-yaml Public
Forked from stephpy/vim-yamlOverride vim syntax for yaml files
Vim Script UpdatedApr 5, 2020 -
deepvariant Public
Forked from google/deepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Python BSD 3-Clause "New" or "Revised" License UpdatedMar 26, 2020 -
truvari Public
Forked from ACEnglish/truvariStructural variant comparison tool for VCFs
Python MIT License UpdatedMar 1, 2019 -
sv-benchmark Public
Forked from PacificBiosciences/sv-benchmarkPublic Benchmark of Long-Read Structural Variant Caller on PacBio CCS HG002 Data
UpdatedFeb 27, 2019 -
SURVIVOR Public
Forked from fritzsedlazeck/SURVIVORToolset for SV simulation, comparison and filtering
C++ MIT License UpdatedNov 21, 2018 -
minimap2 Public
Forked from lh3/minimap2A versatile pairwise aligner for genomic and spliced nucleotide sequences
C MIT License UpdatedJun 4, 2018 -
-
giab_data_indexes Public
Forked from genome-in-a-bottle/giab_data_indexesThis repository contains data indexes from NIST's Genome in a Bottle project.
UpdatedJun 30, 2016 -
Burrow-Wheeler Aligner for pairwise alignment between DNA sequences
C GNU General Public License v3.0 UpdatedDec 14, 2015 -
-
PyVCF Public
Forked from jamescasbon/PyVCFA Variant Call Format reader for Python.
Python Other UpdatedSep 17, 2014
{{ message }}