chd_dnvs

Repository associated with dissection of human cardiac enhancers and congenital heart disease de novo variants using MPRA

https://github.com/pulab/chd_dnvs

Science Score: 44.0%

This score indicates how likely this project is to be science-related based on various indicators:

  • CITATION.cff file
    Found CITATION.cff file
  • codemeta.json file
    Found codemeta.json file
  • .zenodo.json file
    Found .zenodo.json file
  • DOI references
  • Academic publication links
  • Academic email domains
  • Institutional organization owner
  • JOSS paper metadata
  • Scientific vocabulary similarity
    Low similarity (0.5%) to scientific vocabulary
Last synced: 10 months ago · JSON representation ·

Repository

Repository associated with dissection of human cardiac enhancers and congenital heart disease de novo variants using MPRA

Basic Info
  • Host: GitHub
  • Owner: pulab
  • Language: HTML
  • Default Branch: main
  • Size: 35.1 MB
Statistics
  • Stars: 0
  • Watchers: 0
  • Forks: 1
  • Open Issues: 0
  • Releases: 1
Created almost 4 years ago · Last pushed over 2 years ago
Metadata Files
Readme Citation

README.md

CHD_DNVs

Repository associated with dissection of human cardiac enhancers and congenital heart disease de novo variants using MPRA.

Contents:

Owner

  • Login: pulab
  • Kind: user

Citation (CITATION.cff)

# This CITATION.cff file was generated with cffinit.
# Visit https://bit.ly/cffinit to generate yours today!

cff-version: 1.2.0
title: 'MPRA designer, analyzer; EpiCard'
message: >-
  If you use this software, please cite it using the
  metadata from this file.
type: software
authors:
  - given-names: Sarah
    family-names: Morton
  - given-names: Xiaoran
    family-names: Zhang
  - given-names: William
    family-names: Pu
    orcid: 'https://orcid.org/0000-0002-4551-8079'
  - {}
repository-code: 'https://github.com/pulab/CHD_DNVs/releases/tag/V1'
abstract: >-
  Code accompanying article by Xiao, Zhang, Morton, et al.,
  "Functional dissection of human cardiac enhancers and
  non-coding de novo variants in congenital heart disease",
  Nature Genetics 2024

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