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Comment: C: Running iqtree in a python script?
7.2 years ago by DVA ▴ 630
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5.5k
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Comment: C: Develop an R package for CRAN vs BioConductor
7.3 years ago by DVA ▴ 630
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5.5k
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Comment: C: Develop an R package for CRAN vs BioConductor
7.3 years ago by DVA ▴ 630
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5.5k
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Comment: C: Develop an R package for CRAN vs BioConductor
7.3 years ago by DVA ▴ 630
0
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0
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5.5k
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Comment: C: Develop an R package for CRAN vs BioConductor
7.3 years ago by DVA ▴ 630
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0
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5.5k
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Comment: C: Develop an R package for CRAN vs BioConductor
7.3 years ago by DVA ▴ 630
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7.5k
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Comment: C: Extract surrounding genome sequences given certain locations using R
7.3 years ago by DVA ▴ 630
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7.5k
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Comment: C: Extract surrounding genome sequences given certain locations using R
7.3 years ago by DVA ▴ 630
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7.5k
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Comment: C: Extract surrounding genome sequences given certain locations using R
7.3 years ago by DVA ▴ 630
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1.5k
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Comment: C: Convert BLAST NC_ labels to chromosome label
7.3 years ago by DVA ▴ 630
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2.8k
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Comment: C: Large input when using jellyfish
7.5 years ago by DVA ▴ 630
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9.7k
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Comment: C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by DVA ▴ 630
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9.7k
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Comment: C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by DVA ▴ 630
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9.7k
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Comment: C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by DVA ▴ 630
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9.7k
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Comment: C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by DVA ▴ 630
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1.2k
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Comment: C: Filter for Smith_Waterman local alignment algorithm
7.9 years ago by DVA ▴ 630
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10k
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Comment: C: How To Split Reads For Different Flowcell Lanes In Fastq Files?
7.9 years ago by DVA ▴ 630
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3.6k
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Comment: C: Does BWA (BWA-MEM) care about the identity and coverage of the mapped reads?
7.9 years ago by DVA ▴ 630
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4.2k
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Comment: C: about somatic mutation calling
7.9 years ago by DVA ▴ 630
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3.3k
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Comment: C: Non-cancer somatic mutation calling
7.9 years ago by DVA ▴ 630
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1
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3.3k
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Comment: C: Non-cancer somatic mutation calling
7.9 years ago by DVA ▴ 630
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3.3k
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Comment: C: Non-cancer somatic mutation calling
7.9 years ago by DVA ▴ 630
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3.3k
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Comment: C: Non-cancer somatic mutation calling
7.9 years ago by DVA ▴ 630
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1
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4.2k
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Comment: C: about somatic mutation calling
7.9 years ago by DVA ▴ 630
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1
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4.2k
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Comment: C: about somatic mutation calling
7.9 years ago by DVA ▴ 630
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1.3k
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Comment: C: identifying aspecific snp in sequenced genes
7.9 years ago by DVA ▴ 630
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1.5k
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Comment: C: how to query dbsnp locally
8.0 years ago by DVA ▴ 630
2
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3.5k
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Comment: C: mate pair trimming ?
8.0 years ago by DVA ▴ 630
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1.6k
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Comment: C: Extract genotype from hg19
8.2 years ago by DVA ▴ 630
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2.0k
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Comment: C: Can't locate dbSNP 131 anymore?
8.2 years ago by DVA ▴ 630
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2.0k
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Comment: Comment: Can't locate dbSNP 131 anymore?
updated 21 months ago by 43k • written 8.2 years ago by ▴ 630
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4.4k
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Comment: C: Why do people not call normal and tumor variant separately for somatic mutation
8.2 years ago by DVA ▴ 630
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4.4k
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Comment: C: Why do people not call normal and tumor variant separately for somatic mutation
8.2 years ago by DVA ▴ 630
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1
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3.6k
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Comment: C: Manually edit the flags in a sam file
8.6 years ago by DVA ▴ 630
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1
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3.6k
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Comment: C: Manually edit the flags in a sam file
8.6 years ago by DVA ▴ 630
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3.6k
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Comment: Comment: Manually edit the flags in a sam file
updated 19 months ago by 43k • written 8.6 years ago by ▴ 630
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3.6k
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Comment: Comment: Manually edit the flags in a sam file
updated 19 months ago by 43k • written 8.6 years ago by ▴ 630
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6.4k
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Comment: C: Identify point mutations from each read in sam files
8.6 years ago by DVA ▴ 630
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1
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6.4k
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Comment: C: Identify point mutations from each read in sam files
8.6 years ago by DVA ▴ 630
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1
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6.4k
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Comment: Comment: Identify point mutations from each read in sam files
updated 19 months ago by 43k • written 8.7 years ago by ▴ 630
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6.4k
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Comment: C: Identify point mutations from each read in sam files
8.7 years ago by DVA ▴ 630
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4.0k
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Comment: C: Question about Details in Picard MarkDuplicates
8.9 years ago by DVA ▴ 630
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3.7k
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Comment: C: Remove both pair end reads with low mapping quality using Samtools
9.4 years ago by DVA ▴ 630
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3.7k
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Comment: C: Remove both pair end reads with low mapping quality using Samtools
9.4 years ago by DVA ▴ 630
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2.6k
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Comment: Comment: Trouble obtaining chromosome number using standalone blastn
updated 2.3 years ago by 43k • written 9.6 years ago by ▴ 630
95 results • Page 2 of 2
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