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Comment: C: Which Bioinformatic Friendly Pipeline Building Framework?
7.6 years ago by DG 7.3k
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1
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5.7k
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Comment: C: Percentage Of Exons Covered
7.6 years ago by DG 7.3k
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3.6k
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Comment: C: How to call genotype bases for all the samples?
7.7 years ago by DG 7.3k
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2.7k
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Comment: C: How to compare correlations between tumor samples
7.7 years ago by DG 7.3k
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2.5k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.7 years ago by DG 7.3k
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2.5k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.7 years ago by DG 7.3k
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1
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2.7k
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Comment: C: How to compare correlations between tumor samples
7.7 years ago by DG 7.3k
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1
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2.7k
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Answer: A: How to compare correlations between tumor samples
7.8 years ago by DG 7.3k
4
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2.8k
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Answer: A: How to differentiate SNPs Vs Sequencing error in RNA Seq?
7.8 years ago by DG 7.3k
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1
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2.7k
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Comment: C: How to compare correlations between tumor samples
7.8 years ago by DG 7.3k
1
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1
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2.5k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.8 years ago by DG 7.3k
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1.3k
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Answer: A: Biological replicates for transcript profiling, not differential expression
7.8 years ago by DG 7.3k
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1
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2.5k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.8 years ago by DG 7.3k
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2.6k
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Comment: C: Statistical significance in phylogenies
7.8 years ago by DG 7.3k
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2.4k
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Comment: C: Which SNPs fall within genes and what's their description?
7.8 years ago by DG 7.3k
1
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1
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2.6k
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Comment: C: Statistical significance in phylogenies
7.8 years ago by DG 7.3k
1
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1
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2.4k
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Answer: A: Which SNPs fall within genes and what's their description?
7.8 years ago by DG 7.3k
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1.3k
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Comment: C: Acetylation/Methylation relation with genetic diseases
7.8 years ago by DG 7.3k
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1.3k
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Answer: A: Acetylation/Methylation relation with genetic diseases
7.8 years ago by DG 7.3k
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3.1k
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Comment: C: How to read the numbers at the end of a leaf node for my phylogenetic tree?
7.8 years ago by DG 7.3k
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0
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3.1k
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Comment: C: How to read the numbers at the end of a leaf node for my phylogenetic tree?
7.8 years ago by DG 7.3k
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1
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4.1k
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Comment: C: Standalone Multiple Sequence alignment tool
7.8 years ago by DG 7.3k
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1
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2.1k
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Comment: C: variant calling tumor/normal exome sequencing
7.8 years ago by DG 7.3k
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1
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2.1k
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Answer: A: variant calling tumor/normal exome sequencing
7.8 years ago by DG 7.3k
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2.5k
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Comment: C: How to construct multiple sequence alignment from group of pairwise alignments
7.8 years ago by DG 7.3k
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1
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2.5k
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Comment: C: How to construct multiple sequence alignment from group of pairwise alignments
7.8 years ago by DG 7.3k
3
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2.8k
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Answer: A: Help with NGS analysis
7.9 years ago by DG 7.3k
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1
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2.5k
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Answer: A: How to construct multiple sequence alignment from group of pairwise alignments
7.9 years ago by DG 7.3k
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1
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3.6k
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Answer: A: How to call genotype bases for all the samples?
7.9 years ago by DG 7.3k
0
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0
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13k
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Comment: C: how to get the genotypes from vcf file.
7.9 years ago by DG 7.3k
1
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1
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13k
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Comment: C: how to get the genotypes from vcf file.
7.9 years ago by DG 7.3k
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1
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13k
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Comment: C: how to get the genotypes from vcf file.
7.9 years ago by DG 7.3k
2
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4.1k
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Answer: A: Why don't phylogenetic analyses using DNA sequences and protein sequences result
8.0 years ago by DG 7.3k
2
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0
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4.1k
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Comment: C: Why don't phylogenetic analyses using DNA sequences and protein sequences result
8.0 years ago by DG 7.3k
2
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0
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4.4k
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Answer: A: bcftools isec: weird number of output file
8.0 years ago by DG 7.3k
0
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0
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3.6k
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Comment: C: Threshold to exclude samples based on sample-to-sample distances
8.0 years ago by DG 7.3k
0
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1
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3.6k
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Answer: A: Threshold to exclude samples based on sample-to-sample distances
8.0 years ago by DG 7.3k
0
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0
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2.3k
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Answer: A: genes in RAS/MEK pathway
8.0 years ago by DG 7.3k
3
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0
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1.7k
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Comment: C: How can I determine which statistical method is appropriate ?
8.0 years ago by DG 7.3k
1
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1
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4.3k
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Comment: C: Variant Calling in Somatic mode
8.1 years ago by DG 7.3k
2
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1
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4.3k
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Comment: C: Variant Calling in Somatic mode
8.1 years ago by DG 7.3k
0
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0
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4.3k
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Comment: C: Variant Calling in Somatic mode
8.1 years ago by DG 7.3k
1
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1
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4.3k
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Comment: C: Variant Calling in Somatic mode
8.1 years ago by DG 7.3k
5
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1
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7.4k
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Answer: A: MutScan: Detect important mutations by scanning FastQ files directly
8.2 years ago by DG 7.3k
1
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1
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2.1k
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Answer: A: Is there an over representation for cancer processes in pathway databases (e.g.
8.2 years ago by DG 7.3k
0
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0
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95k
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Comment: C: What Is The Best Method To Find Orthologous Genes Of A Species?
8.2 years ago by DG 7.3k
0
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1
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95k
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Comment: C: What Is The Best Method To Find Orthologous Genes Of A Species?
8.2 years ago by DG 7.3k
0
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0
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3.1k
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Comment: C: Need an advice on quality control of illumina reads
8.2 years ago by DG 7.3k
1
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0
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2.5k
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Comment: C: VariantCalling with single sanger read
8.2 years ago by DG 7.3k
1
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1
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2.5k
views
Answer: A: VariantCalling with single sanger read
8.2 years ago by DG 7.3k
835 results • Page 3 of 17
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