A fast and space-efficient pre-filter for estimating the quantification of very large collections of nucleotide sequences
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Updated
Oct 24, 2026 - C++
A fast and space-efficient pre-filter for estimating the quantification of very large collections of nucleotide sequences
is an open-source LIMS (laboratory Information Management System) for Next Generation Sequencing sample management, statistics and reports, and bioinformatics analysis service management.
AI4Bio 生物信息学智能体合集:文献/序列/结构/测序/富集/设计,10 个即装即用
various tools that help with deep sequencing analysis
Detection of CNVs (deletion/duplication) in target panel based NGS data
Data portal and API for Center for Viral Systems Biology (CViSB) data
Mitochondrial DNA sequence assembly and annotation for nematodes using NGS data.
This repository contains a internal web page for sequencing runs management for NextSeq and MiSeq Illumina machines.
iSkyLIMS home website for information and links purposes
1D intervals incremental inverted index
SRSF shape analysis framework for sequencing data
WOLAND is a multiplatform tool to analyze point mutation patterns using resequencing data from any organism or cell. It is implemented as a Perl and R tool using as inputs filtered unannotated or annotated SNV lists, combined with its correspondent genome sequences.
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