Ultimagen
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healthomics-workflows
healthomics-workflows PublicUltimaGenomics repository for workflows compatible with AWS HealthOmics
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VariantCalling
VariantCalling PublicUltima scripts related to downstream processing of WGS, MRD, methylation analysis
Jupyter Notebook 8
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FREEC
FREEC PublicForked from BoevaLab/FREEC
Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data
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picard
picard PublicForked from broadinstitute/picard
A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
Java
Repositories
- healthomics-workflows Public
UltimaGenomics repository for workflows compatible with AWS HealthOmics
Ultimagen/healthomics-workflows’s past year of commit activity - VariantCalling Public
Ultima scripts related to downstream processing of WGS, MRD, methylation analysis
Ultimagen/VariantCalling’s past year of commit activity - gridss Public Forked from PapenfussLab/gridss
GRIDSS: the Genomic Rearrangement IDentification Software Suite
Ultimagen/gridss’s past year of commit activity - wgbs_tools Public Forked from nloyfer/wgbs_tools
tools for working with Bisulfite Sequencing data while preserving reads intrinsic dependencies
Ultimagen/wgbs_tools’s past year of commit activity - picard Public Forked from broadinstitute/picard
A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
Ultimagen/picard’s past year of commit activity - parascopy Public Forked from tprodanov/parascopy
Copy number estimation and variant calling for duplicated genes using WGS.
Ultimagen/parascopy’s past year of commit activity
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