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Fixing Errors in Bam Files
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1
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476
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December 21, 2023
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error: more sample fields than samples listed in header samples
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1
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624
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December 21, 2023
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SnpEff Chromosome Not Found Error
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1
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525
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December 21, 2023
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Error Messages in bcftools
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1
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391
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December 21, 2023
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Assistance with Variant Analysis
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6
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319
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November 21, 2023
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I can't find SNP Primer Design Module
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3
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296
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November 2, 2023
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Please avail the admixture software in GALAXY
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1
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257
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October 30, 2023
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How to use the tool--SNP Primer Design?
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3
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431
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October 18, 2023
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How can I split a VCF file by chromosome?
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2
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2552
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September 14, 2023
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Gubbins failed to giveresults on various galaxy links
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1
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223
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August 31, 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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289
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August 29, 2023
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About INS annoation (snpEff)
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0
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205
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August 10, 2023
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What is the correct input for Stacks: populations??
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6
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443
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July 28, 2023
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Stacks: Using trimmed sequences as input for de novo map?
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2
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286
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July 26, 2023
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Rstudio on Galaxy.eu : installing new packages
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5
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787
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July 6, 2023
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TB-Profiler is not working anymore
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1
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287
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July 6, 2023
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Genome assembly and gene annotation
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1
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232
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June 16, 2023
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Tutorials, tools, and custom reference genomes
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1
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412
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June 6, 2023
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Snippy to find SNP in bacterial DNA seq
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6
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625
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June 5, 2023
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Mapping reads to references by PEAR, bowtie2, samtool idx and sort tools
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4
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418
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June 2, 2023
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gemını inheritance pattern
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1
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407
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May 24, 2023
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problem with bcftools isec
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3
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517
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May 2, 2023
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Convert VCF to pg_snp and gd_snp
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5
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589
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April 13, 2023
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Ways to make a variant calling for RNA Seq (paired-end)
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5
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667
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April 12, 2023
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SnpEff eff: annotate variants is producing errors
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2
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304
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April 1, 2023
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Variant Analysis/ JBrowse
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1
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309
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March 15, 2023
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Errors urgent in variant filtering and insertsize
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2
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495
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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
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879
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February 24, 2023
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Eukaryote VCF annotation
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5
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303
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February 10, 2023
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Error while Intersecting VCF files
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3
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416
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February 4, 2023
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