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Compare 16S samples
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1
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4
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April 3, 2025
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FreeBayes not working with built-in genome
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3
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11
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April 2, 2025
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BWA MEM2 too slow
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9
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37
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April 2, 2025
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Variant calling using snippy
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1
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15
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March 29, 2025
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Haplotype analysis
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7
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16
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March 24, 2025
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galaxy training - Calling variants in diploid systems gemini annotation source unavailable
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8
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37
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March 15, 2025
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Pooled sequecing as Somatic-Germline analysis
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1
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5
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February 19, 2025
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Database?? Human Genealogy
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1
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6
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February 18, 2025
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SNP density visualization
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1
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29
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February 15, 2025
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Cannot access Crispresso2 tool from usegalaxy.org
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3
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7
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February 13, 2025
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Troubleshooting Snippy memory allocation error
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1
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29
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February 4, 2025
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Global change in splicing
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3
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16
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January 15, 2025
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manta SV is generating no output files
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1
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27
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December 21, 2024
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false positives and negatives when long reads corrected using short reads
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2
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12
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November 20, 2024
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I cant visualise any data on my SNPs table
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2
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20
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November 7, 2024
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MiModD Extract Variant Sites - filtering germline
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1
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5
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November 5, 2024
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Variant calling with VarScan on WGS data
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5
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69
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October 12, 2024
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variant's prediction of pathogenicity
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1
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15
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September 17, 2024
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Exome sequencing data analysis for diagnosing a genetic disease: Problem in Finding and reporting plausible causative variants step
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7
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40
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September 5, 2024
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Download of free Bayes vcf files not possible in some cases
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1
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9
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September 4, 2024
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FreeBayes Software Error Report
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2
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18
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August 26, 2024
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problems with vcftools merge command
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2
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563
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August 9, 2024
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Variant annotation and calling
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1
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27
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August 8, 2024
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FilterMutectCalls not avaible on galaxy
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1
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26
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July 31, 2024
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DeepVariant low quality sorting
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1
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58
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July 31, 2024
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Issue with ivar variants Output in Galaxy: Missing Annotations
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1
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18
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July 24, 2024
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1001_Genome project
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1
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20
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July 22, 2024
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Comparing SNPs across samples and sample groups
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3
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36
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July 19, 2024
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snippy analysis on bacterial isolates
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3
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104
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July 17, 2024
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CNV detection from BAM files (mouse)
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1
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118
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July 9, 2024
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