noefp / easy_gdbLinks
☆12Updated 3 weeks ago
Alternatives and similar repositories for easy_gdb
Users that are interested in easy_gdb are comparing it to the libraries listed below
Sorting:
- Collection of utilities for working with PacBio-based assemblies☆13Updated 2 years ago
- The OpEx (Optimised Exome) pipeline☆9Updated 6 years ago
- This is the GPress, a framework for querying GTF, GFF3 and expression files in a compressed form.☆12Updated last year
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Updated 4 years ago
- ClaMSA (Classify Multiple Sequence Alignments).☆13Updated 7 months ago
- A command line tool (in Kotlin/JVM) for intuitively visualizing BAM alignments. (Currently unmaintained)☆10Updated last year
- CLI to automate Nextflow pipeline testing☆12Updated 2 weeks ago
- Nanopore Real-Time Analysis Tool☆15Updated 10 months ago
- SeqWho - A reliable and rapid FASTQ(A) file classifier☆11Updated 3 years ago
- mreps: software for tandem repeat identification in DNA☆14Updated 5 years ago
- Hidden Markov Model based Copy number caller☆20Updated 8 months ago
- Hybrid Error Correction of Long Reads using Iterative Learning☆10Updated 6 years ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 6 years ago
- Scalable and High Performance Variant Calling on Cluster Environments☆10Updated 3 years ago
- Toolkit for calling and analyzing de novo STR mutations☆14Updated last year
- Teaching modules for Human Genome Variation Lab.☆20Updated last month
- Variant call adjudication☆16Updated last year
- A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region exp…☆23Updated 4 months ago
- ☆12Updated 2 months ago
- ☆16Updated 6 months ago
- Bioinformatics tools for dealing with Multiple Alignment Format (MAF) files.☆11Updated last week
- Prioritizing Copy Number Variants (CNV) using Phenotype and Gene Functional Similarity☆16Updated 3 years ago
- Bedfile perturbation tool☆17Updated last year
- ☆9Updated 3 years ago
- AccuSyn: An Accurate Web-based Genome Synteny Browser☆16Updated 10 months ago
- A tool set to assess the quality of the per read phasing and reduce the errors.☆12Updated 5 years ago
- Removing PCR duplicates for sequencing reads.☆14Updated 4 years ago
- Coronavirus (SARS-Cov-2) sequencing analysis☆10Updated 3 years ago
- Benchmarking variant calling in polyploids☆15Updated 3 years ago
- RCK: Reconstruction of clone- and haplotype-specific Cancer Karyotypes☆17Updated 5 years ago