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problems with vcftools merge command
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2
|
578
|
August 9, 2024
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Negative values with VCF filter tool
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6
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502
|
May 13, 2024
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Analysis of splice variants.
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4
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337
|
January 2, 2024
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vcf-sort not found
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1
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513
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December 21, 2023
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Assistance with Variant Analysis
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6
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347
|
November 21, 2023
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Please avail the admixture software in GALAXY
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1
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268
|
October 30, 2023
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How to properly apply filters in VCF annotate
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1
|
725
|
October 30, 2023
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creating a simple variant analysis table
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1
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335
|
October 19, 2023
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Variant calling from VCF files
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3
|
759
|
October 16, 2023
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How can I split a VCF file by chromosome?
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2
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2708
|
September 14, 2023
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A tool in the platform that performs allele frequency calculation on a set of samples?
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1
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332
|
August 29, 2023
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Lofreq returns error
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6
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466
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December 21, 2023
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freebayes parameter selection issue
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2
|
358
|
June 9, 2023
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Tutorials, tools, and custom reference genomes
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1
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414
|
June 6, 2023
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send files from Galaxy to UCSC's EU mirror
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11
|
878
|
May 19, 2023
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Galaxy Plink doesn't accept pbed composite dataset when uploaded from local disk
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3
|
537
|
May 12, 2023
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problem with bcftools isec
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3
|
605
|
May 2, 2023
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Convert VCF to pg_snp and gd_snp
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5
|
601
|
April 13, 2023
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Ways to make a variant calling for RNA Seq (paired-end)
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5
|
811
|
April 12, 2023
|
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Errors urgent in variant filtering and insertsize
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2
|
510
|
March 10, 2023
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VarScan error: index file older than data file and fail to parse certain regions
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2
|
1010
|
February 24, 2023
|
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Eukaryote VCF annotation
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5
|
308
|
February 10, 2023
|
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Error while Intersecting VCF files
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3
|
450
|
February 4, 2023
|
|
Genom not found in SnpEff annotation
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2
|
391
|
January 13, 2023
|
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Filtering SnpEff output with SnpSift
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2
|
1192
|
January 4, 2023
|
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Genotype Quality not visible in VCF file
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2
|
441
|
January 3, 2023
|
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Paired-End RNA Seq Trimming
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5
|
1302
|
December 20, 2023
|
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Variant analysis with MiModD
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2
|
338
|
July 23, 2022
|
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Unable to select VCF with Gemini load? Tool form includes full input requirements
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1
|
742
|
June 21, 2022
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Merging VCF files
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|
3
|
1111
|
June 16, 2022
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