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exome sequencing GEMINI load error
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7
|
847
|
July 23, 2022
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Edit chromosome identifiers in VCF files
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1
|
400
|
May 8, 2022
|
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Naive Variant Caller, Samtools mpileup inaccuracies
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4
|
460
|
April 7, 2022
|
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VCFfilter region - do not want to filter on region
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3
|
463
|
March 11, 2022
|
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Retrieve SNP info from bam files
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3
|
1997
|
March 4, 2022
|
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SnpEff error while processing VCF entry on Galaxy
|
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10
|
1235
|
February 10, 2023
|
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Subsetting VCF by regions in BED
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1
|
652
|
February 5, 2022
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How to annotate VCF files using SnpSift Annotate and dbSNPs?
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2
|
1236
|
February 3, 2022
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KSNP3 annotations error
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0
|
314
|
January 31, 2022
|
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Error in filtering vcf
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2
|
360
|
December 21, 2023
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How to transform 23andme and ancestry's data to VCF?
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1
|
1262
|
February 18, 2025
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MEME-chip question about input format
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1
|
702
|
January 18, 2022
|
|
variant calling samtools
|
|
5
|
1014
|
December 13, 2021
|
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Is there anything available to replace the deprecated Genome Diversity tools
|
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5
|
698
|
November 4, 2021
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Building an indexed genome file for GATK tools
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13
|
2479
|
October 27, 2021
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How can I count the number of reads that support a variant in a vcf file?
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2
|
1026
|
August 30, 2021
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iVar variants - Enhancement request: Include optional GFF3 reference annotation
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4
|
537
|
August 11, 2021
|
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unable to download Snpeff database in Galaxy
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2
|
472
|
December 21, 2023
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