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132 results for source starred repositories
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Short reads aligner for NIPT/CNV

C 15 4 Updated Oct 10, 2018

TraCeR - reconstruction of T cell receptor sequences from single-cell RNAseq data

Python 126 48 Updated Nov 28, 2023

The complete sequence of a human genome

928 99 Updated Nov 19, 2024

Tools (written in C using htslib) for manipulating next-generation sequencing data

C 1,646 580 Updated Dec 12, 2024

A parallel wrapper for LTR_FINDER

Perl 49 12 Updated Jan 8, 2024

Extensive de-novo TE Annotator

Perl 352 74 Updated Dec 3, 2024

A telomere-to-telomere toolkit for gap-free genome assembly and centromeric repeat identification

Python 106 8 Updated Dec 17, 2024

An integrated pipeline for identification of SSR markers

Perl 5 2 Updated Apr 25, 2022

Implementation of the Pairwise Sequentially Markovian Coalescent (PSMC) model

C 156 60 Updated Nov 21, 2022

a hierarchical guided genome assembler

Python 3 1 Updated Jan 7, 2022

Ultrafast de novo assembly for long noisy reads (though having no consensus step)

TeX 309 70 Updated Dec 13, 2023

A single molecule sequence assembler for genomes large and small.

C++ 663 179 Updated Dec 19, 2024

Rapid large-scale prokaryote pan genome analysis

Perl 325 190 Updated Apr 21, 2022

Inference of ploidy and heterozygosity structure using whole genome sequencing data

C 248 24 Updated Dec 2, 2024

Developed for assemble the genomes with second-generation sequencing data, especially using the Illumina short reads. It is comparable to SOAPdenovo, and approach to SOAPdenovo2 in some aspects.

C++ 5 Updated Jul 1, 2020

EndHic is a fast and easy-to-use Hi-C scaffolding tool, using the Hi-C links from contig end regions instead of whole contig regions to assemble large contigs into chromosomal-level scaffolds.

Perl 19 3 Updated Mar 11, 2023

GCE (genomic charactor estimator) is a bayes model based method to estimate the genome size, genomic repeat content and the heterozygsis rate of the sequencing sample. The estimated result can be u…

Roff 48 5 Updated Feb 27, 2020

A pipeline to de novo assemble the stLFR reads using Supernova Assembler

Shell 20 5 Updated Feb 22, 2023

MECAT: an ultra-fast mapping, error correction and de novo assembly tool for single-molecule sequencing reads

C++ 108 26 Updated Oct 2, 2020

A One-Click System for Analyzing Loop-Resolution Hi-C Experiments

Shell 421 183 Updated Nov 22, 2024

Wiki form of BLAST documentation from NCBI

16 2 Updated Feb 21, 2017

NCBI Prokaryotic Genome Annotation Pipeline

Common Workflow Language 321 90 Updated Dec 12, 2024

Rapid & standardized annotation of bacterial genomes, MAGs & plasmids

Python 461 57 Updated Dec 18, 2024

Accurate sample inference from amplicon data with single nucleotide resolution

R 479 144 Updated Dec 4, 2024

A cross-platform and ultrafast toolkit for FASTA/Q file manipulation

Go 1,337 160 Updated Nov 25, 2024

A cross-platform, efficient and practical CSV/TSV toolkit in Golang

Go 1,028 85 Updated Dec 6, 2024

A Practical and Efficient NCBI Taxonomy Toolkit, also supports creating NCBI-style taxdump files for custom taxonomies like GTDB/ICTV

Go 388 32 Updated Nov 14, 2024

Find, circularise and annotate mitogenome from PacBio assemblies

Python 170 30 Updated Aug 8, 2024

hybrid assembly pipeline for bacterial genomes

C++ 572 136 Updated Jul 25, 2024

Trinity RNA-Seq de novo transcriptome assembly

Perl 841 320 Updated Aug 1, 2024
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