campanam / BaitsToolsLinks
Software for hybridization capture bait design
☆11Updated last year
Alternatives and similar repositories for BaitsTools
Users that are interested in BaitsTools are comparing it to the libraries listed below
Sorting:
- Detecting NUMTs from WGS☆13Updated last year
- Structural variant merging tool☆55Updated last year
- Differential quantification of alternative splicing events on spliced pangenome graphs☆14Updated 8 months ago
- Cost-efficient genome-wide gene expression profiling☆16Updated 2 years ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆23Updated 10 years ago
- perSVade: personalized Structural Variation detection☆40Updated last month
- An insertion caller for Illumina paired-end WGS data.☆23Updated last month
- Long read to rMATS☆32Updated 2 years ago
- Analysis of TE contribution to features (transcripts or simple features). Includes utils to test enrichment.☆27Updated 6 years ago
- A stand-alone application for constructing websites for visualizing and browsing synteny blocks☆18Updated 4 years ago
- ☆32Updated last year
- ☆38Updated 2 years ago
- ☆51Updated 6 years ago
- Phylogeny-based Contamination Detection in Mitochondrial and Whole-Genome Sequencing Studies☆18Updated 2 years ago
- An accurate repeat detection from Nanopore data using deep learning and image techniques☆23Updated 2 years ago
- Scripts for analyses and figures for SNP STR Imputation manuscript☆14Updated 7 years ago
- R package to explore active transposable elements with RNA-seq data☆21Updated 2 years ago
- ☆30Updated 4 years ago
- Pipeline for scaffolding and breaking a genome assembly using 10x genomics linked-reads☆21Updated 3 years ago
- This repo is be archived, these workflows are still housed housed in the GATK repository under the scripts directory. The workflows are a…☆22Updated 5 years ago
- Method used in the study on germline mutation rate estimation in 68 species of vertebrates.☆15Updated 4 years ago
- microRNA PREdiction From small RNA-seq data☆29Updated 7 years ago
- A new tool to infer sex from massively parallel sequencing data.☆17Updated 5 months ago
- Method for inferring path posterior probabilities and abundances from pangenome graph read alignments☆57Updated last month
- Identify and annotate TE-mediated insertions in long-read sequence data☆43Updated 3 months ago
- CNEFinder: Finding Conserved Non-coding Elements in Genomes☆25Updated 4 years ago
- Split-read pipeline for the identification of non-reference TE insertions with TSDs☆25Updated 5 years ago
- SQANTI2 is now replaced by SQANTI3. Please go to: https://github.com/ConesaLab/SQANTI3☆38Updated 5 years ago
- processing 10x genomics reads☆26Updated 5 years ago
- Genotype and phase short tandem repeats using Illumina whole-genome sequencing data☆32Updated 4 years ago