Chemical118 / GDBrLinks
Genomic signature interpretation tool for DNA double-strand break repair mechanism
☆11Updated 3 months ago
Alternatives and similar repositories for GDBr
Users that are interested in GDBr are comparing it to the libraries listed below
Sorting:
- 충남대학교 김준 연구실 튜토리얼☆45Updated last year
- 유전학자를 위한 시퀀싱 자료 분석☆23Updated 5 years ago
- Sends alerts to a Slack/Discord channel or an email for potentially interesting new articles selected from RSS feeds.☆54Updated last month
- VcfExplorer regroups several programs which principal aims are to map DNA and RNAseq data onto reference genome sequence, perform variant…☆15Updated last year
- Workflow for identifying and classifying homologous gene/protein sequences☆21Updated 3 months ago
- MGcount github repository☆14Updated 2 years ago
- ☆10Updated last year
- Supplemental code for "the architecture of SARS-CoV-2 transcriptome" paper☆101Updated 5 years ago
- Method used in the study on germline mutation rate estimation in 68 species of vertebrates.☆16Updated 4 years ago
- WITCH is a multiple sequence alignment method that uses multiple weighted HMMs to align unaligned sequences and find consensuses.☆13Updated last month
- Software for hybridization capture bait design☆11Updated last year
- The Genome Analysis Tutorial Page.☆13Updated 6 years ago
- ☆11Updated 5 years ago
- A versatile sequenced read processor for nanopore direct RNA sequencing☆82Updated 5 years ago
- DeepMP is a computational tool to detect DNA modifications in Nanopore sequencing data☆28Updated 3 years ago
- Scripts and code for Kākāpō genomic data☆14Updated 2 years ago
- ☆14Updated 3 years ago
- Differential quantification of alternative splicing events on spliced pangenome graphs☆14Updated 11 months ago
- Transformer-based sequence correction method for genome assembly polishing☆95Updated 10 months ago
- Synteny Mapping and Analysis Program☆30Updated last week
- Clair3-Trio: variant calling in trio using Nanopore long-reads☆16Updated last year
- A repository for the GenGraph toolkit for the creation and manipulation of graph genomes☆51Updated 4 years ago
- Mark duplicate reads from PacBio sequencing of an amplified library☆11Updated 10 months ago
- TransPi – a comprehensive TRanscriptome ANalysiS PIpeline for de novo transcriptome assembly☆28Updated 4 years ago
- VCF Observer is a VCF file analysis, comparison, and visualization tool.