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Reading data into RStudio on DNA Nexus
- Former User of DNAx Community_63
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Do the multiple jobs run simultaneously by default? or does the for loop run everything sequentially?
- Brenton Pyle
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We are interested in exploring the raw accelerometry data (p90001) from physical activity measurements. This data exists inside 'Bulk' folder within our project as files with '.cwa' file extension. How can we open these '.cwa' files in UK-RAP platform?
- Former User of DNAx Community_96
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How to store large genotype/phenotype data on the RAP that will be queried within custom code?
- Former User of DNAx Community_21
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Making PHESANT compatible dataset from participant table
- Former User of DNAx Community_65
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JupyterLab Spark SQL queries keep hanging
- Former User of DNAx Community_62
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UK Biobank Project Data Update Clarification
- Permanently deleted user
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Is there an updated version of plink available with the Swiss Army Knife?
- Former User of DNAx Community_55
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For the chunked population wide 450k WES vcfs, where can one find a position file delimiting the start and end positions of each chunk?
- Former User of DNAx Community_53
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For the WGS, where can I find a list of which samples were sequenced in each cohort (Sanger Main, Sanger Vanguard and deCODE)?
- Permanently deleted user
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Why does VCFtools force the maximum allele filter to 2 on Swiss Army knife? This doesn't happen when running VCFtools outside of DNA Nexus.
- Former User of DNAx Community_46
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Can you annotate with CADD, gnomad, clinvar and dbNSFP options when using hail on Spark jupyterlab notebooks?
- Former User of DNAx Community_4
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Does the EID in the main file matches with the EID in UKB RAP for the same application?
- Former User of DNAx Community_39
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What is the best way to extract a list of variants from WGS data?
- Permanently deleted user
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Where I can find sample codes how to LiftOver genotype data from HG37 to HG38 using Picard LiftOverVCF?
- Permanently deleted user
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What is the best way to label loss-of-function variants to then perform GWAS on LoF variants and phenotypic outcome? Would a SnpEff -> SnpFilt -> Plink2 pipeline make sense? I am new to this type of research!
- Permanently deleted user
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How can we download the "return" associated with a publication?
- Permanently deleted user
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Is HLA imputation available on RAP?
- Permanently deleted user
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Cohort browser - Genomics - AF frequency and count not the same size as the cohort I built
- Former User of DNAx Community_39
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Is there a way to view the spark UI when running jupyter notebooks?
- Former User of DNAx Community_55
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Webinar May 12: Cloud Computing for HPC Users
- Brenton Pyle
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What is the best way to filter each WES VCF using a list of variants of interest and merge the results?
- Former User of DNAx Community_46
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Is there a way to find the record censoring dates for a particular data release version?
- Former User of DNAx Community_57
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Where is dxjupyterlab-vep on spark cluster with HAIL-VEP? Cache is not found either.
- Former User of DNAx Community_4
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Unable to save Hail output files
- Former User of DNAx Community_66
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