DyogenIBENS / FINSURF
FINSURF is a tool designed to analyse lists of sequences variants in the human genome.
☆12Updated 2 years ago
Alternatives and similar repositories for FINSURF:
Users that are interested in FINSURF are comparing it to the libraries listed below
- Immuological gene typing and annotation for genome assembly☆35Updated 2 weeks ago
- Identify and annotate TE-mediated insertions in long-read sequence data☆41Updated last year
- ☆21Updated 3 months ago
- Structural variant merging tool☆49Updated 7 months ago
- ☆17Updated 2 years ago
- TEMP is a software package for detecting transposable elements (TEs) insertions and excisions from pooled high-throughput sequencing dat…☆22Updated 7 years ago
- ☆33Updated last year
- Reconstruction of focal amplifications with long reads☆18Updated this week
- Summarise and plot data from long-read ONT (direct RNA/cDNA) BAM files☆14Updated 11 months ago
- DNA multiple sequence aligner, official version from Penn State's Miller Lab☆31Updated 6 years ago
- A pipeline to detect chimeric transcripts derived from genes and transposable elements.☆23Updated 8 months ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 3 months ago
- heuristics to merge structural variant calls in VCF format.☆36Updated 8 years ago
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- Variant annotation and merging pipeline☆32Updated 2 months ago
- Genotyping of segregating mobile elements insertions☆19Updated 3 years ago
- ☆39Updated 6 months ago
- Pipeline to identify isoforms from full-length cDNA sequencing data☆24Updated 10 months ago
- Genotype and phase short tandem repeats using Illumina whole-genome sequencing data☆30Updated 3 years ago
- ☆29Updated 7 months ago
- toolkit to process gtf files☆17Updated 3 years ago
- processing 10x genomics reads☆25Updated 5 years ago
- ☆18Updated 8 months ago
- ☆23Updated 3 years ago
- A method for measuring chromosome-specific telomere length from long reads☆21Updated 10 months ago
- An accurate repeat detection from Nanopore data using deep learning and image techniques☆22Updated 2 years ago
- Enabling differential allele-specific analysis☆11Updated 3 months ago
- PopSTR - A Population based microsatellite genotyper☆32Updated last year
- ERVcaller is a tool designed to accurately detect and genotype non-reference unfixed endogenous retroviruses (ERVs) and other transposabl…☆13Updated last year
- Master of Pores 2☆23Updated 3 months ago