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Showing results
Python 3 Updated Feb 11, 2020

Code and data to reproduce results from Ruegg et al. paper on the Willow Flycatcher genoscape

R 3 Updated Apr 1, 2021

A course on genomics and bioinformatics from WU

HTML 57 19 Updated Sep 30, 2024

Resources for Brown University's BIOL 1435 course.

Jupyter Notebook 20 Updated May 1, 2024
R 186 25 Updated Jul 28, 2024

Foreign Contamination Screening caller scripts and documentation

101 13 Updated Jun 18, 2024

A (very) simple script to QC Hi-C data.

Python 24 5 Updated Jul 6, 2023
Shell 8 4 Updated Jun 4, 2021

Friends don't let friends make certain types of data visualization - What are they and why are they bad.

R 6,326 230 Updated Jul 11, 2024

Tools and pipelines tailored to using PacBio HiFi Reads for metagenomics

HTML 169 34 Updated Sep 23, 2024

Perform taxonomic profiling analyses for long-read shotgun metagenomic datasets. Developed for the Long Read Sequencing Workshop 2022 at the Jackson Laboratory.

13 2 Updated May 12, 2022

a Bioinformatics Application for Navigating De novo Assembly Graphs Easily

C++ 112 10 Updated Aug 3, 2024

Graphical Fragment Assembly (GFA) Format Specification

Makefile 195 42 Updated Aug 21, 2024

Annotation helper tool for the manual curation of transposable element consensus sequences

R 43 6 Updated May 22, 2024

info and docs for the Wright Lab

14 9 Updated Jan 27, 2016

Only The Best (Genome Assembly Tools)

Nextflow 5 3 Updated Aug 12, 2024

Extracts records from a fasta based on a list of fasta headers.

Python 1 Updated Oct 3, 2023

Visualizing transcript structure and annotation using ggplot2

R 130 9 Updated Aug 24, 2024

A single fast and exhaustive tool for summary statistics and simultaneous *fa* (fasta, fastq, gfa [.gz]) genome assembly file manipulation.

C++ 91 8 Updated Sep 26, 2024

Remove CCS reads with remnant PacBio adapter sequences and convert outputs to a compressed .fastq (.fastq.gz).

Shell 80 19 Updated Jul 23, 2024

Convert .bam to .fastq and remove reads with remnant PacBio adapter sequences

Shell 2 Updated Aug 2, 2021

tools for working with genome variation graphs

C++ 1,097 194 Updated Oct 1, 2024

DeepConsensus uses gap-aware sequence transformers to correct errors in Pacific Biosciences (PacBio) Circular Consensus Sequencing (CCS) data.

Python 223 38 Updated Jun 2, 2023

Align subreads to ccs reads

C++ 13 2 Updated Sep 6, 2023

Telomere-to-telomere assembly of accurate long reads (PacBio HiFi, Oxford Nanopore Duplex, HERRO corrected Oxford Nanopore Simplex) and Oxford Nanopore ultra-long reads.

Python 289 29 Updated Sep 27, 2024

Yet another Hi-C scaffolding tool

C 126 18 Updated Sep 30, 2024

scaffolding based on Hi-C, 10X linked reads, linkage disequilibrium information.

C 5 1 Updated Oct 29, 2020

A quick user guide for de novo transposable element (TE) library generation and TE screening. Utilising; the Extensive de novo TE Annotator (EDTA), DeepTE, RepeatMasker and RM_TRIPS.

R 26 1 Updated Dec 7, 2022

Test sets and pipeline scripts for pan-genomic graph analysis

Python 16 2 Updated Aug 22, 2024
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