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3
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Answer: A: De novo transcript assembly from multiple RNA-seq datasets
8.7 years ago by andrew.j.skelton73 6.6k
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1.6k
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Comment: C: how to identify if RNAseq data is from same patient
8.7 years ago by andrew.j.skelton73 6.6k
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2.6k
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Comment: C: reading microarray data in R
8.7 years ago by andrew.j.skelton73 6.6k
1
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2.7k
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Answer: A: Labelling heatmap dendrogram
8.7 years ago by andrew.j.skelton73 6.6k
2
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3.0k
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Answer: A: Methylation 27K 450K, 850K, 2.5M: Why not plant more probes
8.7 years ago by andrew.j.skelton73 6.6k
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2.6k
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Comment: C: reading microarray data in R
8.7 years ago by andrew.j.skelton73 6.6k
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1.7k
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Comment: C: Corroborate Splicing Variants
8.7 years ago by andrew.j.skelton73 6.6k
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1.7k
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Comment: C: Corroborate Splicing Variants
8.7 years ago by andrew.j.skelton73 6.6k
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2
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1.7k
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Answer: A: Corroborate Splicing Variants
8.7 years ago by andrew.j.skelton73 6.6k
1
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1
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3.9k
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Comment: C: problem loading library in R
8.7 years ago by andrew.j.skelton73 6.6k
1
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1.9k
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Answer: A: capturing phenotypic information in R
8.7 years ago by andrew.j.skelton73 6.6k
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14k
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Comment: C: Limma analysis for multiple groups
8.7 years ago by andrew.j.skelton73 6.6k
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2.0k
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Comment: C: Can someone give me explanation about the output of plink
8.7 years ago by andrew.j.skelton73 6.6k
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0
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2.2k
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Comment: C: Bioconductor Package for import and analysis of Illumina HumanOmni2.5-4v1_c?
8.7 years ago by andrew.j.skelton73 6.6k
1
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1
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2.2k
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Answer: A: Bioconductor Package for import and analysis of Illumina HumanOmni2.5-4v1_c?
8.7 years ago by andrew.j.skelton73 6.6k
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12k
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Comment: C: Why GATK and bcftools SNP calling different?
8.7 years ago by andrew.j.skelton73 6.6k
2
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1
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3.7k
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Answer: A: Can I bulid a new reference for bwa ?
8.7 years ago by andrew.j.skelton73 6.6k
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2.1k
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Comment: C: RNA-Seq reads aligned from Bowtie (not Tophat) is not working with Cuffdiff?
8.7 years ago by andrew.j.skelton73 6.6k
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1
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2.1k
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Comment: C: RNA-Seq reads aligned from Bowtie (not Tophat) is not working with Cuffdiff?
8.7 years ago by andrew.j.skelton73 6.6k
2
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1
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2.7k
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Comment: C: How to decipher FPKM Values?
8.7 years ago by andrew.j.skelton73 6.6k
1
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1
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2.0k
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Comment: C: Interpreting 2 RNA-seq data with different lengths
8.7 years ago by andrew.j.skelton73 6.6k
0
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1
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2.0k
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Answer: A: Interpreting 2 RNA-seq data with different lengths
8.7 years ago by andrew.j.skelton73 6.6k
1
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0
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2.7k
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Comment: C: How to decipher FPKM Values?
8.7 years ago by andrew.j.skelton73 6.6k
0
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1
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2.2k
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Answer: A: IsoDE-bootstrap based differential gene expression analysis for RNASeq data,with
8.7 years ago by andrew.j.skelton73 6.6k
0
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1
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2.9k
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Comment: C: HTSeq error with bam file input
8.7 years ago by andrew.j.skelton73 6.6k
0
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1
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2.9k
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Comment: C: HTSeq error with bam file input
8.7 years ago by andrew.j.skelton73 6.6k
1
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1
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7.2k
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Answer: A: PLINK Principal Components not adequately controlling for population stratificat
8.7 years ago by andrew.j.skelton73 6.6k
0
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0
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3.2k
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Comment: C: How to calculate RPKM using cuffdiff after obtaining accepted_hits.bam?
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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3.2k
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Comment: C: How to calculate RPKM using cuffdiff after obtaining accepted_hits.bam?
8.8 years ago by andrew.j.skelton73 6.6k
0
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0
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1.3k
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Comment: C: Help with 2nd read data analysis
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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1.9k
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Answer: A: Comparing log2 fold values with in a file using a r studio program?
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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3.2k
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Comment: C: How to calculate RPKM using cuffdiff after obtaining accepted_hits.bam?
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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3.2k
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Answer: A: How to calculate RPKM using cuffdiff after obtaining accepted_hits.bam?
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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2.5k
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Comment: C: 80% of FPKM values are zero after cufflinks
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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1.7k
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Answer: A: drop levels in eSet pData
8.8 years ago by andrew.j.skelton73 6.6k
1
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0
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8.1k
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Comment: C: Amzon EC2 for bioinformatics, genomics, NGS analysis
8.8 years ago by andrew.j.skelton73 6.6k
3
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2
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8.1k
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Answer: A: Amzon EC2 for bioinformatics, genomics, NGS analysis
8.8 years ago by andrew.j.skelton73 6.6k
1
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0
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1.8k
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Comment: C: Filtering out mutations from cancer dataset
8.8 years ago by andrew.j.skelton73 6.6k
0
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0
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2.3k
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Answer: A: How can overdominant genotype model contribute to disease risk?
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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3.1k
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Comment: C: RNAseq comparisons (tophat->HTSeq->edgeR) return only a few sig diffs, and all s
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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3.1k
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Comment: C: RNAseq comparisons (tophat->HTSeq->edgeR) return only a few sig diffs, and all s
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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3.1k
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Comment: C: RNAseq comparisons (tophat->HTSeq->edgeR) return only a few sig diffs, and all s
8.8 years ago by andrew.j.skelton73 6.6k
0
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0
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13k
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Comment: C: Why Does The Base Quality Drop Towards The End For Illumina Reads ?
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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13k
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Answer: Answer: Why Does The Base Quality Drop Towards The End For Illumina Reads ?
updated 2.4 years ago by 44k • written 8.8 years ago by 6.6k
2
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0
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2.0k
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Answer: Answer: How to further process inSilicoMerging data in R?
updated 2.4 years ago by 44k • written 8.8 years ago by 6.6k
0
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1
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3.8k
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Comment: C: Duplicate gene symbols converted from UCSC gene id
8.8 years ago by andrew.j.skelton73 6.6k
0
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1
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4.4k
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Comment: Comment: Recalling SNPs count from Illumina SNP array raw data
updated 2.4 years ago by 44k • written 8.8 years ago by 6.6k
0
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1
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4.4k
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Answer: Answer: Recalling SNPs count from Illumina SNP array raw data
updated 2.4 years ago by 44k • written 8.8 years ago by 6.6k
0
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1
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4.4k
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Comment: Comment: limma: blocking for batch/individual in paired samples with multiple tissues
updated 2.4 years ago by 44k • written 8.8 years ago by 6.6k
1
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1
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2.2k
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Answer: Answer: my experimental design for cuffdiff
updated 2.4 years ago by 44k • written 8.8 years ago by 6.6k
701 results • Page 11 of 15
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