FelixKrueger / SNPsplit

Allele-specific alignment sorting
http://felixkrueger.github.io/SNPsplit/
GNU General Public License v3.0
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Which reference genome I have to use it for genomepreparation #54

Closed luckysardar closed 3 years ago

luckysardar commented 3 years ago

Greetings.., Nice tool I wanted use SNP split in my chipseq data I am new to this tool Can you please suggest me which reference file I can use here I have downloaded the vcf file v5 from the Sanger database as mentioned in user guide and reference genome from the ensemble GRCm39 latest version with GTF.

Can you please suggest can I proceed with the genome preparation or please suggest link to download reference genome and GTF it will be very helpful

Thank you

luckysardar commented 3 years ago

Hello can you please suggest me...

Thank you

FelixKrueger commented 3 years ago

Sorry for the late response (it turns out that Wales is truly off-grid :)).

The Mouse Genomes Project v5 file requires the GRCm38 genome build (ftp://ftp.ensembl.org/pub/release-102/fasta/mus_musculus/dna/).

luckysardar commented 3 years ago

Thank you for the reply but in VCF file reference mentioned as below comment so I am bit confused can you please clarify

reference=ftp://ftp-mouse.sanger.ac.uk/ref/GRCm38_68.fa

FelixKrueger commented 3 years ago

The important part is that you get the GRCm38 reference sequence. This sequence has not changed since the day it was released. The things that did change are the annotation releases (in your case the _68, I think right now it is >100), however this never affects the DNA sequence itself. Just make sure it is not NCBIM37 or GRCm39.

luckysardar commented 3 years ago

Thank you for the quick reply, Okay In case of GTF which file I have use? below link will work? GRCm38_102

FelixKrueger commented 3 years ago

The GTF file you are going to use might affect your downstream analysis, but will have nothing to do with the SNPsplit processing itself. So yea, the more recent the better I guess?

luckysardar commented 3 years ago

Okay Felix your sggestions will be very helpfull I am using same annotation file for all my analysis RNA and Chip seq so I am believing it will not effect much in my analysis

Thank you.,