Pinned Repositories
EpigenomicsMethylationDataProcessor
BioinformaticsScripts
control_tiempo_cbu
CourseraScripts
funnSV
Functional annotation of Structural Variants (SVs) in vcf format using gff annotated transcriptomes.
MUNCH
Metabolic Unified Network Creation and Handler tool
Personal
pysam
Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.
NGSEPcore
NGSEP is an integrated framework for analysis of high throughput sequencing (HTS) reads. The main functionality of NGSEP is the variants detector, which allows to make integrated discovery and genotyping of Single Nucleotide Variants (SNVs), insertions, deletions, and genomic regions with copy number variation (CNVs).
GenomeAnonymizer
ngaitan55's Repositories
ngaitan55/funnSV
Functional annotation of Structural Variants (SVs) in vcf format using gff annotated transcriptomes.
ngaitan55/MUNCH
Metabolic Unified Network Creation and Handler tool
ngaitan55/BioinformaticsScripts
ngaitan55/CourseraScripts
ngaitan55/EpigenomicsMethylationDataProcessor
ngaitan55/control_tiempo_cbu
ngaitan55/Personal