broadinstitute / flipbook
A tool that lets you quickly flip through images in a local directory and record notes or answer questions about each one.
☆19Updated 3 months ago
Alternatives and similar repositories for flipbook:
Users that are interested in flipbook are comparing it to the libraries listed below
- SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel☆25Updated last week
- TRGT Repeat expansion summary☆10Updated 2 years ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆32Updated last year
- Pipeline code for creating a fully haplotype-resolved assembly from a combination of PacBio/ONT long reads and Illumina Strand-seq data☆16Updated last year
- Structural variant (SV) analysis tools☆36Updated 10 months ago
- Structural variant benchmark☆17Updated 2 months ago
- Variant annotation and merging pipeline☆34Updated last month
- ☆21Updated 3 weeks ago
- Location of public benchmarking; primarily final results☆18Updated 2 months ago
- ☆39Updated 8 months ago
- A long-read analysis toolbox for cancer and population genomics☆23Updated 2 months ago
- Swipe your Structural Variants called on long (ONT/PacBio) reads with short exact (Illumina) reads.☆32Updated 2 years ago
- Dynamic time warping of Oxford Nanopore squiggle data to characterize tandem repeats.☆32Updated 4 years ago
- Working space for the GIAB TR benchmarking project☆21Updated 6 months ago
- StrVCTVRE, a structural variant classifier for exonic deletions and duplications☆18Updated last year
- Tumour-only somatic mutation calling using long reads☆26Updated 6 months ago
- A VCF comparison engine for structual variant benchmarking☆20Updated last year
- Short Tandem Repeat disease loci resource☆18Updated this week
- A module for improving the insertion sequences of structural variant calls☆30Updated 3 years ago
- VCF files of SVs using long-read sequencing (LRS).☆22Updated 3 years ago
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆37Updated 10 months ago
- ☆19Updated 2 months ago
- Miscellaneous scripts for applications of PacBio systems☆27Updated 3 years ago
- Detect and phase minor SNVs from long-read sequencing data☆14Updated 3 years ago
- ☆48Updated 10 months ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆29Updated 10 months ago
- ☆34Updated 5 years ago
- Method to optimally select samples for validation and resequencing☆27Updated 4 years ago
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- Lightweight mosaic/somatic SV caller for long reads (WIP)☆28Updated 5 months ago