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Pooled sequecing as Somatic-Germline analysis
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1
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4
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February 19, 2025
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Database?? Human Genealogy
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1
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4
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February 18, 2025
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SNP density visualization
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1
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18
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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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6
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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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18
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February 4, 2025
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Global change in splicing
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3
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14
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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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14
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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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11
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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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18
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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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4
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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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50
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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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14
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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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35
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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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8
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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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532
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August 9, 2024
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Variant annotation and calling
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1
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22
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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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17
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July 31, 2024
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DeepVariant low quality sorting
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1
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49
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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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16
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July 24, 2024
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1001_Genome project
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1
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13
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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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29
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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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62
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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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92
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July 9, 2024
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Will Nanopore-related tools be updated to accept pod5 files?
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2
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159
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July 8, 2024
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Is Gatk/4.4.0.0 avialble in galaxy?
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1
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142
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May 28, 2024
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FreeBayes variant calling and Snpeff variant annotation
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19
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424
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September 17, 2024
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bcftools view problem
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2
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116
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May 20, 2024
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Identifying polymorphisms in mapped RNA seq data and the corresponding genes
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1
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71
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May 10, 2024
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FTDNA BAM to T2T pileup and haplogroup
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2
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193
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May 7, 2024
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