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Stars

Scientific programming

97 repositories

Accurate sample inference from amplicon data with single nucleotide resolution

R 486 145 Updated Feb 4, 2025

R toolkit for single cell genomics

R 2,388 931 Updated Feb 26, 2025

R toolkit for inference, visualization and analysis of cell-cell communication from single-cell data

R 676 155 Updated Jan 6, 2024

Make Complex Heatmaps

R 1,353 231 Updated Dec 19, 2024

R package for community ecologists: popular ordination methods, ecological null models & diversity analysis

R 473 99 Updated Feb 28, 2025

phyloseq is a set of classes, wrappers, and tools (in R) to make it easier to import, store, and analyze phylogenetic sequencing data; and to reproducibly share that data and analysis with others. …

R 597 189 Updated Apr 29, 2024

(No maintenance) Next Generation Sequencing Simulation with SNP, Variation and Sequencing Error Integrated

Julia 24 10 Updated Aug 10, 2017

Processing and analysis of data coming from Illumina sequencing machines

Perl 9 17 Updated Feb 27, 2025

An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)

C++ 2,023 332 Updated Nov 28, 2024

A collection of sequencing protocols and bioinformatic resources for SARS-CoV-2 sequencing.

Perl 347 87 Updated Apr 12, 2023

Cutadapt removes adapter sequences from sequencing reads

Python 537 132 Updated Feb 17, 2025

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

C 1,683 582 Updated Feb 28, 2025

Next generation sequencing reads de novo assembler.

C 228 77 Updated Dec 24, 2023

RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.

Nextflow 990 728 Updated Mar 7, 2025

A repository for setting up a RNAseq workflow

R 427 181 Updated Apr 10, 2017

A PyTorch Basecaller for Oxford Nanopore Reads

Python 403 123 Updated Jul 25, 2024

Megalodon is a research command line tool to extract high accuracy modified base and sequence variant calls from raw nanopore reads by anchoring the information rich basecalling neural network out…

Python 198 29 Updated May 4, 2023

Sequence correction provided by ONT Research

Python 437 77 Updated Oct 11, 2024

Read trimming tool for Illumina NGS data.

Java 131 91 Updated Mar 10, 2015

Viral genomics analysis pipelines

Python 192 67 Updated Sep 20, 2024

QC checks and metrics for Illumina NGS data

Perl 5 18 Updated Feb 20, 2025

k-mer based Pipeline to identify the Serotype from Illumina NGS reads

Python 21 19 Updated Jul 13, 2023

Community-curated list of software packages and data resources for single-cell, including RNA-seq, ATAC-seq, etc.

3,320 1,006 Updated Feb 25, 2025

Open-source bioinformatics components for Dash

Python 540 191 Updated Feb 13, 2025

Collection of bioinformatics training materials

Python 1,007 183 Updated Feb 23, 2025

Windowed Adaptive Trimming for fastq files using quality

C 218 96 Updated May 8, 2017

SKESA assembler

C++ 115 20 Updated Oct 11, 2024

Tools and pipelines tailored to using PacBio HiFi Reads for metagenomics

HTML 183 35 Updated Feb 12, 2025

AutoDock Vina

C++ 680 230 Updated Mar 5, 2025

Welcome to the mothur project, initiated by Dr. Patrick Schloss and his software development team in the Department of Microbiology & Immunology at The University of Michigan. This project seeks to…

C++ 271 110 Updated Jan 21, 2025