Nils Homer (nh13)

nh13

Geek Repo

Company:@fulcrumgenomics

Home Page:https://www.linkedin.com/in/nilshomer

Twitter:@nilshomer

Github PK Tool:Github PK Tool


Organizations
bioconda
conda-forge
conda-incubator
fulcrumgenomics
nf-core
samtools

Nils Homer's starred repositories

website

Code and files for the main nf-core website.

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stitch

Stitch is a toolkit for analysis of chimeric reads in sequencing data

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plasmapR

Creating plasmid maps inside ggplot.

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latch

a python bioinformatics framework

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pgr-tk

PGR-TK: Pangenome Research Tool Kit

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gget

🧬 gget enables efficient querying of genomic reference databases

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aegea

Amazon Web Services Operator Interface

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stix

Structural Variant Index

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fgpyo

Quality of life improvements for Bioinformatics in Python.

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hmcnc

Hidden Markov Model based Copy number caller

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extendr

R extension library for rust designed to be familiar to R users.

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GLIMPSE

Low Coverage Calling of Genotypes

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perbase

Per-base per-nucleotide depth analysis

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calitas

This repository is home to CALITAS, a CRISPR-Cas-aware ALigner for In silico off-TArget Search. CALITAS implements a customized gapped alignment of guide sequences to genomes and other reference sequences, returning consistent and non-redundant alignments.

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CoSA

Coronavirus (SARS-Cov-2) sequencing analysis

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sv-cnv-studies

:books: Relevant papers for CNV and SV approaches

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WFA-paper

Wavefront alignment algorithm (WFA): Fast and exact gap-affine pairwise alignment

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GenomicSQLite

Genomics Extension for SQLite

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snakemake-pytest

Snakemake with pytest example

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conda-env-builder

Build and maintain multiple custom conda environments all in one place.

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samwell

Samwell: a python package for using genomic files... well

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Ribo-seQC

A comprehensive analysis tool for Ribo-seq and small RNA-seq data

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pyfgaws

Python tools and APIs for working with AWS

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samwell

Samwell: a python package for using genomic files... well

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miniwdl

Workflow Description Language developer tools & local runner

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bwa-mem2

The next version of bwa-mem

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