ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data

Overview of attention for article published in Genome Medicine, February 2021

Altmetric Badge

About this Attention Score

Good Attention Score compared to outputs of the same age (65th percentile)

Mentioned by

twitter: 7 X users

f1000: 1 research highlight platform

Citations

dimensions_citation: 41 Dimensions

Readers on

mendeley: 79 Mendeley

Summary X Research highlights Dimensions citations

So far, Altmetric has seen 7 X posts from 7 X users, with an upper bound of 21,371 followers.

RT @markjcowley: @holtjma amen! https://t.co/aG0nEvPK2m https://t.co/LiVla3dRbd

Reply Repost Favourite

@holtjma amen! https://t.co/aG0nEvPK2m https://t.co/LiVla3dRbd

Reply Repost Favourite

#ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data Implements #CNVnator & #Lumpy + sophisticated call filtering for sensitive detection https://t.co/slqgJ7TmpO https://t.co/v5I2DQp1wT

Reply Repost Favourite

RT @4130chromo: ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data https://t.co/0enwonSe…

Reply Repost Favourite

This page shows the most recent X posts that mention this research output.

Click here to find out how to access more activity, including 3 additional X posts.