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8.0k
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Comment: C: Z-Score On Raw Counts
12.6 years ago by Sean Davis 27k
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8.0k
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Comment: C: Z-Score On Raw Counts
12.6 years ago by Sean Davis 27k
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4.3k
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Comment: C: How Can I Make A Multi Alignment From The Vcf File Of Snp'S.
12.6 years ago by Sean Davis 27k
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2.8k
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Answer: A: What'S The Meaning Of Variant Filtering Parameter 'Read Position'?
12.6 years ago by Sean Davis 27k
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4.3k
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Answer: A: How Can I Make A Multi Alignment From The Vcf File Of Snp'S.
12.6 years ago by Sean Davis 27k
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18k
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Comment: C: How To Merge Gff Files
12.6 years ago by Sean Davis 27k
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2
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7.1k
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Comment: C: Finding Differentially Expressed Genes Across Multiple Cell Types In A Datset
12.6 years ago by Sean Davis 27k
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7.1k
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Comment: C: Finding Differentially Expressed Genes Across Multiple Cell Types In A Datset
12.6 years ago by Sean Davis 27k
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7.1k
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Answer: A: Finding Differentially Expressed Genes Across Multiple Cell Types In A Datset
12.6 years ago by Sean Davis 27k
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5.5k
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Comment: C: How To Calculate The P-Value Of Mirna Between Two Samples
12.6 years ago by Sean Davis 27k
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5.5k
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Comment: C: How To Calculate The P-Value Of Mirna Between Two Samples
12.6 years ago by Sean Davis 27k
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5.5k
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Answer: A: How To Calculate The P-Value Of Mirna Between Two Samples
12.6 years ago by Sean Davis 27k
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6.5k
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Answer: A: Rna Seq Cell Type Specificity
12.6 years ago by Sean Davis 27k
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6.5k
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Comment: C: Rna Seq Cell Type Specificity
12.6 years ago by Sean Davis 27k
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9.3k
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Answer: A: Problems With Analysis Of Small Rnaseq Data - Adapter Trimming
12.6 years ago by Sean Davis 27k
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1
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6.5k
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Comment: C: Rna Seq Cell Type Specificity
12.6 years ago by Sean Davis 27k
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1
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2.1k
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Answer: A: Correlation Matrix Considering Sample'S Class
12.6 years ago by Sean Davis 27k
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3.7k
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Comment: C: How To Determine Structural Variant Type Or Reformat Breakpoint Data To Bam
12.6 years ago by Sean Davis 27k
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1
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5.7k
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Answer: A: Impact Of Microarray Gene Expression Normalization On Clustering
12.6 years ago by Sean Davis 27k
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1
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4.4k
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Comment: C: Heterogeneous Snp
12.6 years ago by Sean Davis 27k
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1
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4.4k
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Comment: C: Heterogeneous Snp
12.6 years ago by Sean Davis 27k
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3.0k
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Answer: A: How To Retrieve Allele Frequency For A Large Data ?
12.6 years ago by Sean Davis 27k
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1
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4.9k
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Comment: C: Help In Writing A Perl Script To Call Somatic Variants
12.6 years ago by Sean Davis 27k
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1
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4.9k
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Comment: C: Help In Writing A Perl Script To Call Somatic Variants
12.6 years ago by Sean Davis 27k
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1
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4.1k
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Answer: Answer: How To Get Genotype/Variation Information From Geo Gse Data Set In R
updated 3.1 years ago by 45k • written 12.7 years ago by 27k
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4.0k
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Comment: Comment: How To Get Significant Genes From Microarray Experiments Data In Geo
updated 4.6 years ago by 45k • written 12.7 years ago by 27k
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3.7k
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Comment: C: Matching Ensemble Ids In Input And Library File Using R
12.7 years ago by Sean Davis 27k
2
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1
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4.0k
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Answer: Answer: How To Get Significant Genes From Microarray Experiments Data In Geo
updated 4.6 years ago by 45k • written 12.7 years ago by 27k
2
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2
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3.7k
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Answer: A: Matching Ensemble Ids In Input And Library File Using R
12.7 years ago by Sean Davis 27k
6
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0
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17k
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Answer: A: How To Plot A Circular Genome Map?
12.7 years ago by Sean Davis 27k
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4.3k
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Comment: C: How To Simulate Whole-Exome Reads
12.7 years ago by Sean Davis 27k
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5.9k
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Comment: C: Rrna Removal In Rna-Seq Data
12.7 years ago by Sean Davis 27k
1
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1
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4.3k
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Comment: C: How To Simulate Whole-Exome Reads
12.7 years ago by Sean Davis 27k
0
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1
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4.3k
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Comment: C: How To Simulate Whole-Exome Reads
12.7 years ago by Sean Davis 27k
1
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0
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3.8k
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Answer: A: Permutation Test For Cdna Microarray
12.7 years ago by Sean Davis 27k
0
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1
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3.8k
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Comment: C: Permutation Test For Cdna Microarray
12.7 years ago by Sean Davis 27k
1
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1
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3.8k
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Answer: A: Frma Normalization Via Insilicodb
12.7 years ago by Sean Davis 27k
0
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1
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3.8k
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Comment: C: Permutation Test For Cdna Microarray
12.7 years ago by Sean Davis 27k
1
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0
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11k
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Comment: C: Tophat: Compressed Fastq File (Gz)
12.7 years ago by Sean Davis 27k
1
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0
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8.6k
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Answer: A: Clustering Gene Absence And Presence Data In Binary Format
12.7 years ago by Sean Davis 27k
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0
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9.8k
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Comment: C: How To Separate Strands In Sequencing Data Obtained Via Directional Rna-Seq Libr
12.7 years ago by Sean Davis 27k
0
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1
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9.8k
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Comment: C: How To Separate Strands In Sequencing Data Obtained Via Directional Rna-Seq Libr
12.7 years ago by Sean Davis 27k
1
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1
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9.8k
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Answer: A: How To Separate Strands In Sequencing Data Obtained Via Directional Rna-Seq Libr
12.7 years ago by Sean Davis 27k
0
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1
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3.5k
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Comment: C: How To Putatively Identify Intronic Regions/Splice Sites Based On Sequence In Li
12.7 years ago by Sean Davis 27k
2
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15k
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Answer: A: Plotting Read Densities And Gene Tracks In R?
12.7 years ago by Sean Davis 27k
0
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1
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9.8k
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Comment: C: How To Separate Strands In Sequencing Data Obtained Via Directional Rna-Seq Libr
12.7 years ago by Sean Davis 27k
4
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2.7k
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Answer: A: Hierarchical Clustering
12.7 years ago by Sean Davis 27k
3
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16k
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Answer: A: Which Type Of Database Systems Are More Appropriate For Storing Information Extr
12.7 years ago by Sean Davis 27k
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7.4k
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Comment: C: Coverage For Pair-End Rna-Seq, Extend Reads Or Not?
12.7 years ago by Sean Davis 27k
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0
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2.6k
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Comment: C: Low Empirical Scores For Exome Data While Base Quality Sscore Recalibration In G
12.7 years ago by Sean Davis 27k
1,985 results • Page 25 of 40
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