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2
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4.5k
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Comment: C: best workflow for RNA data analysis without replications
updated 4.3 years ago by 43k • written 8.3 years ago by ▴ 360
0
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0
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1.8k
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Comment: C: Variable selection for multiple regression from large number of predictors
updated 4.4 years ago by 43k • written 8.3 years ago by ▴ 360
0
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1
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4.3k
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Comment: C: Disadvantage of RNA-seq compared with Microarray?
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
1
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0
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4.9k
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Comment: C: Heatmap of Differentially Expressed Genes
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
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1
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3.7k
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Comment: C: MEGAN: Exported number of assigned reads is actually the summarized hits
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
1
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1
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3.0k
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Comment: C: Merging bam files
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
0
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0
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1.8k
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Comment: C: Finding the largest possible combination of mutations
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
2
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0
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6.3k
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Comment: C: best alignment tool for Ion Torrent data
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
3
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0
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6.1k
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Comment: C: RNA-Seq Analysis: To sort or not to Sort?
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
0
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1
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6.1k
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Comment: C: RNA-Seq Analysis: To sort or not to Sort?
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
0
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0
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4.4k
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Comment: C: how to convert R contingency table to a matrix that will be used to merge with o
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
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0
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2.0k
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Comment: C: Customised calling of heterozygous snp
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
1
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0
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3.2k
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Comment: Comment: How to correct invalid genotype in ped file ?
updated 20 months ago by 43k • written 8.4 years ago by ▴ 360
1
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0
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7.9k
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Comment: C: extracting heterozygous snp from a vcf file
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
0
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0
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7.9k
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Comment: C: How to filter short length blast results from output
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
0
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1
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4.1k
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Comment: C: Get multiple snps coverage (allelic depth) from bam files
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
0
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1
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4.1k
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Comment: C: Get multiple snps coverage (allelic depth) from bam files
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
1
vote
1
reply
7.9k
views
Comment: C: How to filter short length blast results from output
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 360
0
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0
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5.7k
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Comment: C: GSEA using clusterProfiler
5.0 years ago by mkulecka ▴ 360
0
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0
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2.6k
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Comment: C: Error in SAMseq analysis with R
5.5 years ago by mkulecka ▴ 360
1
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0
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39k
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Comment: C: Pca From Vcf Files
6.1 years ago by mkulecka ▴ 360
0
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0
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2.8k
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Comment: C: Merge multiple vcf files while preserving FILTER information
6.4 years ago by mkulecka ▴ 360
0
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1
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2.3k
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Comment: C: usearch version, which one use to get results faster?
7.4 years ago by mkulecka ▴ 360
0
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0
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1.4k
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Comment: C: list variants that map to a genomic location
7.7 years ago by mkulecka ▴ 360
0
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0
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2.7k
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Comment: C: Very slow Bio-linux on VirtualBox?
7.8 years ago by mkulecka ▴ 360
0
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1
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3.5k
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Comment: C: SnpSift annotate outputs invalid files?
8.4 years ago by mkulecka ▴ 360
1
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0
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1.8k
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Comment: C: what happens with htseq-count when several lines in a gff has the same ID?
8.4 years ago by mkulecka ▴ 360
0
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1
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6.3k
views
Comment: C: best alignment tool for Ion Torrent data
8.4 years ago by mkulecka ▴ 360
0
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0
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3.2k
views
Comment: C: VCF file REF Column outputs all 'N'
8.4 years ago by mkulecka ▴ 360
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