From the Base Position track description page you can enter motifs to highlight, edit the amino acid reading frames display, and even add a title to the Browser image. More tools... More …

The STR sequence template file published in 2016 as part of the considerations from the DNA Commission of the International Society for Forensic Genetics on minimal STR sequence …

This page contains links to sequence and annotation downloads for the genome assemblies featured in the UCSC Genome Browser. Downloads are also available via our JSON API, …

This directory contains a dump of the UCSC genome annotation database for the Dec. 2013 (GRCh38/hg38) assembly of the human genome (hg38, GRCh38 Genome Reference …

Beginning with this release, the UCSC Genome Browser version numbers for the human assemblies now match those of the GRC to minimize version confusion. Hence, the GRCh38 …

This data set contains the genomic locations of cytobands based on both the latest build of the human genome (GRch38) and the latest update to the International Standard for human …

Locus information_D5S818 ... (*)Repeat sequences represent all four possible permutations (e.g. AGAT is used for AGAT, GATA, ATAG or TAGA). The first alphabetic representation of the …

Coordinates for GRCh38 chromosomes. A tibble that represents the coordinates for GRCh38 genome assembly, reporting the chromosome label, from and to (chromosome range), the …

Hi, I'm trying to understand the difference between the coordinate systems of different software: UCSC's LiftOver, dbSNP and NCBI Remap. I've a list of SNPs with genomic coordinates in …

The Genome Reference Consortium's human genome assembly version 38 (GRCh38) is the latest version of the GRC human genome reference. The GRCh38 assembly is referred to as …