ok sounds good. thank you! any instructions/info on how to get introns as well?
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I tried running it for mapk1. I entered the region I found through the browser and resulted 1619 variants, not the 6777. Thanks!
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Can you give me specific coordinates that you are using and let me know where your 6777 count comes from
When I look at our vcf file in ftp://ftp.1000genomes.ebi.ac.uk/vol1...ease/20110521/
laura@pg-trace-001[20110521]:tabix ALL.chr22.phase1_release_v3.20101123.snps_indels_svs.genotypes.vcf.gz 22:22108789-22221970 | cut -f1-8
There is only 1591 sites and only 1532 of them are snps
thanks
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those are the results when i use the online converter. but we decided to use the script instead of the online converter so i wouldn't have to save the data onto my computer.
i'm trying to run the script again for the converter and it won't work. i downloaded the vcf to perl converter mentioned above and ran this script:
perl vcf_to_ped_converter.pl -vcf ftp://ftp.1000genomes.ebi.ac.uk/vol1...notypes.vcf.gz -sample_panel_file ftp://ftp.1000genomes.ebi.ac.uk/vol1...L.sample_panel -region 13:32889611-32973805 -population GBR -population FIN
and got this as a result:
Can't open perl script "vcf_to_ped_convert": No such file or directory
I'm assuming I installed/downloaded the script wrong. Am i correct?
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Provide full path to where the script file was downloaded when you try to run the commandOriginally posted by strongside24 View Post
i'm trying to run the script again for the converter and it won't work. i downloaded the vcf to perl converter mentioned above and ran this script:
perl vcf_to_ped_converter.pl -vcf ftp://ftp.1000genomes.ebi.ac.uk/vol1...notypes.vcf.gz -sample_panel_file ftp://ftp.1000genomes.ebi.ac.uk/vol1...L.sample_panel -region 13:32889611-32973805 -population GBR -population FIN
Code:perl [COLOR="Red"]/full_path_to/[/COLOR]vcf_to_ped_converter.pl -vcf ftp://ftp.1000genomes.ebi.ac.uk .....
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Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
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