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download gnomad vcf.bgz.tbi dataset into galaxy for gemini annotate and/or join functions
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2
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317
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January 23, 2020
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Galaxy Tool Wrappers for GATK 4?
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1
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301
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January 13, 2020
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ANNOVAR annotation error
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1
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472
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January 1, 2020
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Use Galaxy to find SNPs between two yeast genome fastq data
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2
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711
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December 22, 2019
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How to filter rare variants (10%) out
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4
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264
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September 18, 2019
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Can I assemble 1 chromosome only with RNA-Star -- Custom Genome, Variant calling, RNA-seq
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2
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283
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September 4, 2019
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BCFtools Mpileup Qual=0
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6
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989
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August 20, 2019
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Calculating variant allele frequency from FreeBayes VCF
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3
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2190
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July 4, 2019
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Generating consensus sequence from bam file re: Variant analysis
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1
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494
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June 20, 2019
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Pileup to consensus sequence aligned to reference - Please help
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2
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1189
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May 10, 2019
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Help With Choice of Nanopore Sequence Data Analysis Tools
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0
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727
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May 5, 2019
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Creating gVCF file by using Galaxy
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0
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205
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March 19, 2019
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When does in-file metadata matter, and what tools on galaxy can help me do so?
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7
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518
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March 15, 2019
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From FastQ to fasta - WGS Variant Analysis
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2
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1101
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February 14, 2019
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Pruning big files - Filtering SNPs
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1
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877
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February 5, 2019
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Regarding Understanding Quality of Mutation
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2
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272
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December 19, 2018
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Change pileup to vcf format allowing for great depth (100.000 reads)???
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1
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650
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December 6, 2018
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Mpileup with vcf output? How to change galaxy to older version?
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3
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633
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December 6, 2018
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