8000 elisefeld (Elise Hachfeld) / Starred · GitHub
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Starred repositories

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A curated list of deep learning image classification papers and codes

2,980 602 Updated Apr 20, 2022

A series of Jupyter notebooks that walk you through the fundamentals of Machine Learning and Deep Learning in Python using Scikit-Learn, Keras and TensorFlow 2.

Jupyter Notebook 29,005 13,087 Updated Jun 13, 2024

The Washington Post is compiling a database of every fatal shooting in the United States by a police officer in the line of duty since 2015.

1,134 510 Updated Jun 17, 2025

basic walk-throughs for alignment and variant calling from NGS sequencing data

216 65 Updated Jan 10, 2025

Count bases in BAM/CRAM files

CMake 319 98 Updated Jan 31, 2022

Official code repository for GATK versions 4 and up

Java 1,818 606 Updated Jul 9, 2025

web-based analysis tool for rare disease genomics

Python 189 90 Updated Jul 3, 2025

Workflows used for processing whole genome sequence data + germline variant calling. This Repository has been archived, please visit the link the ReadMe to obtain the latest version of the workflow.

WDL 28 42 Updated Jan 4, 2021

Variant Calling Pipeline Using GATK4 and Nextflow

Nextflow 56 49 Updated Feb 16, 2023

A structural variation pipeline for short-read sequencing

Python 189 75 Updated Jul 8, 2025

This Snakemake pipeline implements the GATK best-practices workflow

Python 254 145 Updated Jun 8, 2023

A very simple and basic shell script to run GATK best practice pipeline

Shell 2 Updated Sep 2, 2019

Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtool…

Cython 835 289 Updated Jun 16, 2025

Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data

Perl 72 8 Updated Sep 4, 2024

This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html

C 778 249 Updated Jun 30, 2025

The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants

Perl 492 157 Updated Jul 8, 2025

Bayesian haplotype-based genetic polymorphism discovery and genotyping.

C++ 836 267 Updated May 31, 2025

Tesseract Open Source OCR Engine (main repository)

C++ 68,024 10,009 Updated Jul 6, 2025

Leaked GPTs Prompts Bypass the 25 message limit or to try out GPTs without a Plus subscription.

Python 2,296 375 Updated Jan 17, 2024

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

Python 3,447 756 Updated May 16, 2025

List of Computer Science courses with video lectures.

69,320 9,338 Updated Jul 2, 2025

tools for genetic genealogy and the analysis of consumer DNA test results

Python 169 26 Updated Mar 17, 2025

Source code for Gramps Genealogical program

Python 2,566 463 Updated Jul 6, 2025

A python interface for genealogical tools (Geni, RootsMagic, GEDCOM, Family Search...)

Python 35 10 Updated Mar 28, 2021

Open Data Sources

510 190 Updated May 8, 2018

A topic-centric list of HQ open datasets.

63,662 10,159 Updated Nov 13, 2024

An index of all open-source data

JavaScript 4,699 454 Updated Dec 24, 2023

Data and code behind the articles and graphics at FiveThirtyEight

Jupyter Notebook 17,116 11,141 Updated Feb 25, 2025

Simple R API wrapper for the Open Library API

R 12 1 Updated Feb 10, 2021

Curated list of R API wrappers

R 11 3 Updated Aug 28, 2017
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