minimap2
Here are 29 public repositories matching this topic...
simplified cellranger for long-read data
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Sep 18, 2024 - Python
WebAssembly modules for genomics
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Sep 18, 2024 - HTML
Genome-on-Diet is a fast and memory-frugal framework for exemplifying sparsified genomics for read mapping, containment search, and metagenomic profiling. It is much faster & more memory-efficient than minimap2 for Illumina, HiFi, and ONT reads. Described by Alser et al. (preliminary version: https://arxiv.org/abs/2211.08157).
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Sep 4, 2024 - Roff
Detect and quantify plasmid DNA contamination in sequencing data
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Aug 21, 2024 - Python
Rust bindings to minimap2 library
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Aug 20, 2024 - Rust
Repository for variant calling utilizing bioinformatics tools and databases
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Jul 9, 2024
Mitochondrial Long-read Iterative Assembly
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Jun 4, 2024 - Python
Viral genome coverage evaluation for metagenomic diagnostics 🩸
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Sep 20, 2024 - Rust
This repository streamlines the conversion of raw DNA sequencing data from FASTQ to BAM format, incorporating scripts that not only facilitate BAM conversion but also generate Sequence Alignment Map (SAM) files.
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Nov 26, 2023
GateSeeder is the first near-memory CPU-FPGA co-design for alleviating both the compute-bound and memory-bound bottlenecks in short and long-read mapping. GateSeeder outperforms Minimap2 by up to 40.3×, 4.8×, and 2.3× when mapping real ONT, HiFi, and Illumina reads, respectively.
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Oct 3, 2023 - C
Real-time species-typing visualisation for nanopore data.
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Apr 11, 2023 - JavaScript
SneakySnake:snake: is the first and the only pre-alignment filtering algorithm that works efficiently and fast on modern CPU, FPGA, and GPU architectures. It greatly (by more than two orders of magnitude) expedites sequence alignment calculation for both short and long reads. Described in the Bioinformatics (2020) by Alser et al. https://arxiv.o…
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Mar 31, 2023 - VHDL
Converts a part of an alignment (.PAF perhaps others sometimes) to a Circos image using BED and fasta files.
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Jan 21, 2023 - Python
The first work to provide a comprehensive survey of a prominent set of algorithmic improvement and hardware acceleration efforts for the entire genome analysis pipeline used for the three most prominent sequencing data, short reads (Illumina), ultra-long reads (ONT), and accurate long reads (HiFi). Described in arXiv (2022) by Alser et al. https…
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Jun 14, 2022
A lightweight library for working with PAF (Pairwise mApping Format) files
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May 3, 2022 - Python
Scalable and High Performance Variant Calling on Cluster Environments
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Feb 13, 2022 - Python
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