Extremely fast BAM depth calculation for WGS, exome, or targeted sequencing
☆13Jan 25, 2019Updated 7 years ago
Alternatives and similar repositories for bam2bedGraph2
Users that are interested in bam2bedGraph2 are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- hight performance & useful tools for working with fastq and bam files☆28Jan 25, 2019Updated 7 years ago
- ☆11Sep 23, 2022Updated 3 years ago
- Whole organelle genome-wide alignment construction method, which ultilizes BLAST tool, to facilitate phylogeny analysis☆11May 7, 2018Updated 8 years ago
- MrMosaic (Genomic Mosaic Structural Variant Caller)☆15Jul 21, 2017Updated 9 years ago
- CNV detection tool for WES data☆13Aug 21, 2024Updated 2 years ago
- Deploy open-source AI quickly and easily - Special Bonus Offer • AdRunpod Hub is built for open source. One-click deployment and autoscaling endpoints without provisioning your own infrastructure.
- Benchmarking of CNV calling tools☆20May 18, 2019Updated 7 years ago
- This repository contains information about ongoing analysis performed by GIAB☆14Aug 30, 2019Updated 7 years ago
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆51Oct 14, 2023Updated 2 years ago
- ☆11Jun 14, 2023Updated 3 years ago
- filtering trio-based genetic variants in VCFs for clinical review☆22Aug 18, 2020Updated 6 years ago
- VCF files of SVs using long-read sequencing (LRS).☆22Dec 17, 2021Updated 4 years ago
- SMN1 copy-number and sequence variant analysis from next generation sequencing data