Gabaldonlab / perSVade
perSVade: personalized Structural Variation detection
☆39Updated 2 months ago
Alternatives and similar repositories for perSVade
Users that are interested in perSVade are comparing it to the libraries listed below
Sorting:
- Workflow to prepare high accuracy single molecule consensus sequences from amplicon data using unique molecular identifiers☆33Updated last year
- A program for assessing the T2T genome continuity☆73Updated 3 weeks ago
- A Nextflow pipeline for evaluating assembly quality☆33Updated last week
- A Nextflow workflow to generate lift over files for any pair of genomes☆65Updated last month
- De novo annotation of young retrotransposons☆48Updated 3 years ago
- Computational Analysis of Gene Expression Evolution☆40Updated last month
- PhyloAcc a software to detect the changes of conservation of a genomic region☆30Updated last month
- Copy number variant caller and depth visualization utility for PacBio HiFi reads☆41Updated 6 months ago
- PacBio BAM toolkit☆43Updated 2 months ago
- BITACORA: A Bioinformatics tool for gene family annotation☆43Updated last year
- MCHelper: An automatic tool to curate transposable element libraries☆36Updated last month
- ☆43Updated 8 years ago
- dnaPipeTE (for de-novo assembly & annotation Pipeline for Transposable Elements), is a pipeline designed to find, annotate and quantify T…☆55Updated 2 years ago
- A tool for the recovery of unassembled telomeres from soft-clipped read alignments.☆36Updated last month
- A shiny application to visualize MCscan result☆36Updated 2 years ago
- TSEBRA: Transcript Selector for BRAKER☆47Updated 6 months ago
- A tool for evaluate long-read de novo assembly results☆46Updated 8 months ago
- Annotation helper tool for the manual curation of transposable element consensus sequences☆48Updated 2 months ago
- Converts a VCF file to a FASTA alignment provided a reference genome and a GFF file☆49Updated 7 months ago
- A local-haplotagging-based small and structural variant caller☆76Updated last week
- A battery of methylation tools for PacBio HiFi reads☆34Updated 2 months ago
- A genome annotation pipeline that use short and long sequencing reads alignments from animal genomes☆29Updated last year
- Error correction of ONT transcript reads☆58Updated last year
- catalog for long-read sequencing tools☆32Updated 2 years ago
- WDL workflows for variant calling and assembly using ONT☆33Updated last week
- ☆32Updated 4 years ago
- 🚀 LiftOn: Accurate annotation mapping for GFF/GTF across assemblies☆94Updated 2 months ago
- Splitting of sequence reads by internal adapter sequence search☆51Updated last year
- An R package to visualize chromosome scale repeat patterns and predict centromere locations.☆29Updated 7 months ago
- methods for orphan gene prediction paper optimization☆25Updated 3 years ago