ok sounds good. thank you! any instructions/info on how to get introns as well?
Unconfigured Ad
Collapse
X
-
-
I tried running it for mapk1. I entered the region I found through the browser and resulted 1619 variants, not the 6777. Thanks!
Comment
-
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
Comment
-
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?
Comment
-
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 .....
Comment
Latest Articles
Collapse
-
by SEQadmin2
CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).
Despite this, “CRISPR helped turn genome editing from a specialized technique into...-
Channel: Articles
07-31-2026, 11:01 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 08-20-2026, 11:17 AM
|
0 responses
16 views
0 reactions
|
Last Post
by SEQadmin2
08-20-2026, 11:17 AM
|
||
|
Started by SEQadmin2, 08-18-2026, 10:05 AM
|
0 responses
24 views
0 reactions
|
Last Post
by SEQadmin2
08-18-2026, 10:05 AM
|
||
|
Started by SEQadmin2, 08-13-2026, 12:22 PM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
08-13-2026, 12:22 PM
|
||
|
Started by SEQadmin2, 08-11-2026, 10:35 AM
|
0 responses
33 views
0 reactions
|
Last Post
by SEQadmin2
08-11-2026, 10:35 AM
|
Comment