Pinned Repositories
acfs
A pipeline for de novo circRNA identification
ACMG
AGOUTI
Annotated Genome Optimization Using Transcriptome Information
atac_dnase_pipelines
ATAC-seq and DNase-seq processing pipeline
bio-vcf
Smart VCF parser DSL
Bioinformatics
Bioinformatics analysis scripts, workflows, general code examples
cellranger
10x Genomics Single Cell 3' Gene Expression and VDJ Assembly
checkMyIndex
Search for a set of compatible indexes for your sequencing experiment
chip-seq-pipeline
ENCODE Uniform processing pipeline for ChIP-seq
merlin
MERLIN performs common pedigree analyses. Input files describe relationships between individuals in your dataset, store marker genotypes, disease status and quantitative traits and provide information on marker locations and allele frequencies. MERLIN supports input files in either QTDT or LINKAGE format. Although the two formats are very similar, in the discussion below we will focus on QTDT format.
mlebeur's Repositories
mlebeur/ACMG
mlebeur/bio-vcf
Smart VCF parser DSL
mlebeur/Civicdb
mlebeur/clinvar
mlebeur/dbSNP
mlebeur/denovodb
mlebeur/Ensembl_genes
mlebeur/ensembl_regulatory
mlebeur/ensembltorefseq
mlebeur/Exac
mlebeur/Exac_constraints
mlebeur/GDI
mlebeur/gnomad_exome
mlebeur/gnomad_genome
mlebeur/GnomadConstraints
mlebeur/GWAScatalog
mlebeur/HGNC
mlebeur/KEGG
mlebeur/mitomap
mlebeur/mygene.info
MyGene.info: A BioThings API for gene annotations
mlebeur/myvariant.info
MyVariant.info: A BioThings API for human variant annotations
mlebeur/NCBIGene
mlebeur/OMIM
mlebeur/Orphanet
mlebeur/Refseq_gene
mlebeur/scores
mlebeur/test5
BioThings Studio tutorial
mlebeur/testingdepositdata
mlebeur/thousandgenomes
mlebeur/variantDB