There are 1 repository under bedtools topic.
gia: Genomic Interval Arithmetic
Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores and annotations from popular disease databases. Seave stores genomic variation of all types and sizes, and allows filtering for specific inheritance patterns, quality values, allele frequencies and gene lists. Seave is open source and deployable locally, or on a cloud computing provider, and works readily with gene panel, exome and whole genome data, scaling from single labs to multi-institution scale.
RNAseq pipeline for alternative splicing junctions
Detecting transposable element invasions without repeat library. Detects also horizontal transfer events and endogenized viruses. All you need is a reference genome and some short reads
A beginner’s guide to Bioinformatics
program to make bed12 files from bed 6 files based on the name col of the bed6 file.
Useful NGS utilities for everyday use in the form of stand-alone tool.
A public, web-based homozygosity mapping tool
Assembly of RNA transcriptome, differential expression analysis, identification of lncRNA candidates based on genomic context and protein coding potential.
bedtools environment containerized for singularity
bionano annovar annotation
An R-package for daily tasks required to handle biological data as well as avoid re-coding of small functions for quick but necessary data management.
Project for the course of Computational Human Genomics, held by Francesca Demichelis (a.y. 2021-2022) @ University of Trento
How do I automate extracting multiple gene sequences from multiple genomes?
Codes i wrote for the paper "genomic resources for Mediterranean fishes"
Various bioinformatics tools in one package
Sequencing data preprocessing