ok, thanks, so the genomic coordinates of the genes are the same in hg and GRCh ?
Hi all,
What is the difference between GRCh and hg? I have small RNA interaction data with genome like below and they have used hg19 for mapping the reads. I want to use GTF file in Ensemble which is based on GRCh. but I was wondering the hg and GRCh are the same? If not, where can I find the GTF file for the hg19?
chromosome start end interaction ID alignment score of target part strand
chr2 1.9E+08 1.9E+08 human08246 32 +
chr16 5.2E+07 5.2E+07 human04514 32 -
chr3 1.1E+08 1.1E+08 human11115 36 +
chrM 14360 14382 human08122 34 +
2 answers
I believe the genomic content for the two is identical, except for the mitochondrial contig.
The contig names are also different. GRCh37 names them `chr1`, `chr2`,,`chr3`, etc, while hg19 just has `1`, `2`, `3`.
Thus you can use the same GTF file for both (excluding mitochondrial, of course) if you do a simple replace operation for the contig names.
and some degenerate bases have been replaced by 'N' for chr3 and chrY. see: http://plindenbaum.blogspot.fr/2013/07/g1kv37-vs-hg19.html
Although this is basically true, GRCh37 has a number of patches, which won't be included in hg19.
More information to add (courtesy MatthewP): GRCh37 / hg19 / b37 / humanG1Kv37 - Human Reference Discrepancies
In essence: GRCh37 is identical to hg19 on the main contigs (chr1-24), but differ on chrM.
Kevin
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see: Differences Between Reference Human Genome Assemblies From Different Sources
But still, I couldn't figure it out whether hg and GRCh is the same or not. Could you please elaborate more?
Can I make a similar answer in here? Might be useful to others too. If its innapropiate take the according action to fix it, sorry.
Which is the difference between Homo_sapiens.GRCh38.91 and Homo_sapiens.GRCh38.78? Can I use a Homo_sapiens.GRCh38.91.bed as annotation to a genome referenced to Homo_sapiens.GRCh38.78?
Thanks in advance.
The term "GRCh38" refers to the genomic assembly. The ".78" and ".91" refer to the version of gene annotation provided by Ensembl, i.e. where do introns/exons/etc start and end. To my knowledge, the genomic sequence for "GRCh38.78" and "GRCh38.91" should be identical and only the gene annotation should differ.
In GRCh37.91, what does that .91 mean?
see C: what is the difference between GRCh37 and hg19 ?
Hi Pierre..thanks for the link...I am sorry that I am still confused because when I google GRCh37.91, it does not show up...that ''.91'' comes along only with GRCh38. I understand that GRCh37 is the older version than GRCh38. But is that '0.91' a 'Patch'? If so, can it be used for both GRCh 37 or GRCh38?
Thanks for your help
Hi Pierre..thanks for the link...I am sorry that I am still confused because when I google GRCh37.91, it does not show up...that ''.91'' comes along only with GRCh38. I understand that GRCh37 is the older version than GRCh38. But is that '0.91' a 'Patch'? If so, can it be used for both GRCh 37 or GRCh38?
Thanks for your help