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Comment: C: Nextflow using existing Conda Environments
3.8 years ago by bruce.moran ▴ 960
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7.8k
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Comment: C: Nextflow using existing Conda Environments
3.9 years ago by bruce.moran ▴ 960
1
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1
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7.8k
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Comment: C: Nextflow using existing Conda Environments
3.9 years ago by bruce.moran ▴ 960
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1
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2.0k
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Comment: C: How to increase RAM for R scripts run in computer cluster
3.9 years ago by bruce.moran ▴ 960
1
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1
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1.5k
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Comment: C: Empty network file with ARACNe-AP
3.9 years ago by bruce.moran ▴ 960
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2.3k
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Comment: C: RNA Seq Analysis:Feature Counts are zero
3.9 years ago by bruce.moran ▴ 960
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1.5k
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Comment: A: Empty network file with ARACNe-AP
3.9 years ago by bruce.moran ▴ 960
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1
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2.3k
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Comment: C: RNA Seq Analysis:Feature Counts are zero
3.9 years ago by bruce.moran ▴ 960
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1
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1.5k
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Comment: C: Empty network file with ARACNe-AP
3.9 years ago by bruce.moran ▴ 960
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1
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2.3k
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Comment: C: RNA Seq Analysis:Feature Counts are zero
3.9 years ago by bruce.moran ▴ 960
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1
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2.3k
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Comment: C: RNA Seq Analysis:Feature Counts are zero
3.9 years ago by bruce.moran ▴ 960
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1
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2.3k
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Comment: C: RNA Seq Analysis:Feature Counts are zero
3.9 years ago by bruce.moran ▴ 960
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1
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1.6k
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Comment: C: TCGAbiolinks problem downloading ASCAT2 data
3.9 years ago by bruce.moran ▴ 960
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3.7k
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Comment: C: Setting up environment for RNASeq on university HPCC CondaHTTPError: HTTP 000 CO
3.9 years ago by bruce.moran ▴ 960
1
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1
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3.7k
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Comment: C: Setting up environment for RNASeq on university HPCC CondaHTTPError: HTTP 000 CO
3.9 years ago by bruce.moran ▴ 960
0
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1
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1.7k
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Comment: C: Custom matrix building using R from a datafram
3.9 years ago by bruce.moran ▴ 960
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1
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1.7k
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Comment: C: Custom matrix building using R from a datafram
3.9 years ago by bruce.moran ▴ 960
0
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0
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927
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Comment: C: creating container - should it contain a workflow manager?
3.9 years ago by bruce.moran ▴ 960
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1
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1.7k
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Comment: C: TCGA biolinks: peripheral blood healthy control
4.0 years ago by bruce.moran ▴ 960
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1
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1.7k
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Comment: C: Custom matrix building using R from a datafram
4.0 years ago by bruce.moran ▴ 960
1
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2
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4.3k
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Comment: C: Recommendation for packages for cell type deconvolution from bulk RNAseq data?
4.0 years ago by bruce.moran ▴ 960
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1
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1.7k
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Comment: C: Custom matrix building using R from a datafram
4.0 years ago by bruce.moran ▴ 960
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2.3k
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Comment: C: Discrepancy in number of pseudoaligned reads for read quantification with Kallis
4.0 years ago by bruce.moran ▴ 960
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1
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2.3k
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Comment: C: Discrepancy in number of pseudoaligned reads for read quantification with Kallis
4.0 years ago by bruce.moran ▴ 960
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1.2k
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Comment: C: Whole human genome sequence of COVID19 patient
4.1 years ago by bruce.moran ▴ 960
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2
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1.2k
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Comment: C: Whole human genome sequence of COVID19 patient
4.1 years ago by bruce.moran ▴ 960
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1.1k
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Comment: C: Reformat my txt file
updated 4.1 years ago by 43k • written 4.1 years ago by ▴ 960
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1
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1.1k
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Comment: C: Reformat my txt file
4.1 years ago by bruce.moran ▴ 960
1
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2.3k
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Comment: C: Recommendations for Whole Genome Sequencing Workflow
4.2 years ago by bruce.moran ▴ 960
1
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0
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934
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Comment: C: Classifying normal vs cancer tissues from mutational data
4.2 years ago by bruce.moran ▴ 960
1
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1
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934
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Comment: C: Classifying normal vs cancer tissues from mutational data
4.3 years ago by bruce.moran ▴ 960
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4.2k
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Comment: C: How to download BCL files from NextSeq run?
4.7 years ago by bruce.moran ▴ 960
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1.7k
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Comment: C: Need help understanding ARACNe-AP output
4.8 years ago by bruce.moran ▴ 960
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0
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1.5k
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Comment: C: Ploidy for variant calling in tumor pooled samples for amplicon next-generation
4.9 years ago by bruce.moran ▴ 960
0
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1
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4.9k
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Comment: C: GATK4 VariantRecalibrator resource error
5.0 years ago by bruce.moran ▴ 960
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1
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4.9k
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Comment: C: GATK4 VariantRecalibrator resource error
5.0 years ago by bruce.moran ▴ 960
3
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1
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15k
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Comment: C: How to calculate Tumor Mutation Burden (TMB) for TCGA samples
5.1 years ago by bruce.moran ▴ 960
1
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1
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2.5k
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Comment: C: Microsatellite Instability, Whole exome sequencing
5.1 years ago by bruce.moran ▴ 960
0
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0
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5.0k
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Comment: C: low unique mapping ratio of RNA-seq data
5.2 years ago by bruce.moran ▴ 960
0
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1
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5.0k
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Comment: C: low unique mapping ratio of RNA-seq data
5.2 years ago by bruce.moran ▴ 960
0
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1
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5.0k
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Comment: C: low unique mapping ratio of RNA-seq data
5.2 years ago by bruce.moran ▴ 960
1
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2
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1.2k
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Comment: C: Unequally pooling libraries for RNAseq?
5.2 years ago by bruce.moran ▴ 960
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0
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2.9k
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Comment: C: So frustrated compiling necessary packages in a linux system
5.5 years ago by bruce.moran ▴ 960
1
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2.9k
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Comment: C: So frustrated compiling necessary packages in a linux system
5.5 years ago by bruce.moran ▴ 960
0
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1
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2.9k
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Comment: C: So frustrated compiling necessary packages in a linux system
5.5 years ago by bruce.moran ▴ 960
0
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0
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1.7k
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Comment: C: MarkDuplicates RG ID on SAMRecord not found in header
5.6 years ago by bruce.moran ▴ 960
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0
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4.1k
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Comment: C: Can genomicranges do bedtools-like intersection operations?
5.9 years ago by bruce.moran ▴ 960
0
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1
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4.1k
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Comment: A: Can genomicranges do bedtools-like intersection operations?
5.9 years ago by bruce.moran ▴ 960
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2
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4.1k
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Comment: C: Can genomicranges do bedtools-like intersection operations?
5.9 years ago by bruce.moran ▴ 960
1
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0
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5.1k
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Comment: C: EPIC array annotation
5.9 years ago by bruce.moran ▴ 960
102 results • Page 1 of 3
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