From 7c85c4bd3370b68770ff23e0f7763f215b38afef Mon Sep 17 00:00:00 2001 From: David Rogers Date: Tue, 18 Jun 2024 13:41:13 -0700 Subject: [PATCH] fix: update T2T consortia text (#4059) (#4060) --- explorer/files/anvil-catalog/files/consortia/t2t.mdx | 2 -- 1 file changed, 2 deletions(-) diff --git a/explorer/files/anvil-catalog/files/consortia/t2t.mdx b/explorer/files/anvil-catalog/files/consortia/t2t.mdx index 064799f59..a07f210b8 100644 --- a/explorer/files/anvil-catalog/files/consortia/t2t.mdx +++ b/explorer/files/anvil-catalog/files/consortia/t2t.mdx @@ -5,5 +5,3 @@ Leveraging PacBio HiFi sequencing and Oxford Nanopore ultra-long reads, the CHM1 CHM13v1 unlocks complex regions of the genome for clinical and functional study. Additionally, the T2T-CHRY Workspace utilizes the T2T-CHM13v2.0, which provides the first complete sequence for a human Y chromosome from a separate donor (HG002). T2T-CHM13v2.0 was also used as a reference genome for investigating short-read variant calling, incorporating data from the 1000 Genomes Project and the Simons Genome Diversity Project. Another effort from the T2T consortium is the T2T-GreatApes Project which employs PacBio HiFi and Oxford Nanopore ultra-long reads, advancing our understanding of great ape genomics. It evaluates the impact of T2T-chrXY assemblies on read alignments and variant calling across 129 individuals from 11 great ape subspecies, providing reference genomes for various ape species. - -The 1000 Genomes Project, launched in January 2008, is an international research effort to establish variation profiles across the human population. This open access data set continues to be a valuable resource to geneticists.