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2
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Answer: Answer: interpretation of RNA secondary structure
updated 2.6 years ago by 44k • written 9.7 years ago by ★ 4.8k
0
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2
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4.6k
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Comment: Comment: interpretation of RNA secondary structure
updated 2.6 years ago by 44k • written 9.7 years ago by ★ 4.8k
0
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0
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Comment: C: TCGA miRNA data - is this an appropriate approach?
9.8 years ago by Sam ★ 4.8k
3
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1
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2.0k
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Answer: Answer: Annovar: how to update sequence length based on deletion size
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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Comment: Comment: statistical test to see if DE genes cluster around a chromosomal location?
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
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3.1k
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Comment: Comment: Understanding my SNP data
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
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3.1k
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Comment: C: Co-localization of two proteins and interaction
9.8 years ago by Sam ★ 4.8k
1
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0
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13k
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Answer: Answer: compare two data frames column to column
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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0
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13k
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Comment: C: compare two text files column to column
9.8 years ago by Sam ★ 4.8k
0
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1
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3.1k
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Comment: C: Co-localization of two proteins and interaction
9.8 years ago by Sam ★ 4.8k
0
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1
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3.1k
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Answer: Answer: Co-localization of two proteins and interaction
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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0
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5.7k
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Comment: Comment: How to differentiate snps into missense, none and silent using Annovar?
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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1
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5.7k
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Comment: Comment: How to differentiate snps into missense, none and silent using Annovar?
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
1
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1
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5.7k
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Answer: A: How to differentiate snps into missense, none and silent using Annovar?
9.8 years ago by Sam ★ 4.8k
0
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1
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3.6k
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Answer: Answer: EdgeR: different values in expression and differential expression tables
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
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3.6k
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Comment: Comment: EdgeR: different values in expression and differential expression tables
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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1
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26k
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Comment: Comment: p value and adjusted p value in microarray data analysis
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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2
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26k
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Comment: Comment: p value and adjusted p value in microarray data analysis
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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1
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26k
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Comment: Comment: p value and adjusted p value in microarray data analysis
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
2
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1
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26k
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Answer: Answer: p value and adjusted p value in microarray data analysis
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
0
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1
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3.4k
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Comment: Comment: Can I map SNPs without a reference genome?
updated 2.6 years ago by 44k • written 9.8 years ago by ★ 4.8k
1
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1
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3.3k
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Comment: C: Single Cell RNA-seq and validation
9.8 years ago by Sam ★ 4.8k
0
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1
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14k
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Comment: Comment: What is the acceptable % of reads that map to no feature (in RNASeq)?
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
0
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1
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14k
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Comment: Comment: What is the acceptable % of reads that map to no feature (in RNASeq)?
updated 2.6 years ago by 44k • written 9.9 years ago by ★ 4.8k
0
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0
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2.0k
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Answer: Answer: Randomize CDS While Maintaining Amino Acid Sequence
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
0
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0
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2.0k
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Comment: C: Randomize CDS While Maintaining Amino Acid Sequence
9.9 years ago by Sam ★ 4.8k
4
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0
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5.7k
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Answer: A: Rationale for including a certain number of PCs in a GWAS study?
9.9 years ago by Sam ★ 4.8k
1
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2
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4.2k
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Comment: Comment: BLAST result showing greater sequence length in %identities than that of the que
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
1
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1
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3.8k
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Comment: C: PLINK analysis for case/control studies
9.9 years ago by Sam ★ 4.8k
0
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1
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4.2k
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Comment: Comment: BLAST result showing greater sequence length in %identities than that of the que
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
1
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0
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7.3k
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Comment: Comment: How to set a threshold for coefficient of variation in RNA-seq?
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
0
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1
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7.3k
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Comment: C: How to set a threshold for coefficient of variation in RNA-seq?
9.9 years ago by Sam ★ 4.8k
3
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1
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2.8k
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Comment: C: Error in code
9.9 years ago by Sam ★ 4.8k
0
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1
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2.9k
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Comment: C: What tools to map partial reads on genome?
9.9 years ago by Sam ★ 4.8k
1
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2
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2.9k
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Comment: C: What tools to map partial reads on genome?
9.9 years ago by Sam ★ 4.8k
0
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0
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3.0k
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Comment: Comment: running tophat+cufflinks but result in 0 FPKMs
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
0
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0
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12k
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Comment: Comment: Map genetic mutations to protein domain/structure
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
2
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1
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12k
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Answer: Answer: Map genetic mutations to protein domain/structure
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
0
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0
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3.6k
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Comment: Comment: RNA-Seq comparing transcript levels between samples and between experimental run
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
1
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0
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9.8k
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Answer: Answer: Running bowtie2-2.2.3 to create an index
updated 2.7 years ago by 44k • written 9.9 years ago by ★ 4.8k
0
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0
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3.7k
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Comment: Comment: Alignment Tools for Gene Coexpression Networks
updated 2.9 years ago by 44k • written 10.0 years ago by ★ 4.8k
0
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1
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2.8k
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Comment: C: Data management/annotation solutions for microarray and NGS experiments
10.0 years ago by Sam ★ 4.8k
0
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0
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4.9k
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Comment: C: Configurattion for RNAseq analysis and Genome annotation and assembled of Eukari
10.0 years ago by Sam ★ 4.8k
0
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1
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12k
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Comment: Comment: Filtering gene expression correlation matrix in R
updated 2.8 years ago by 44k • written 10.1 years ago by ★ 4.8k
0
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1
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12k
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Comment: Comment: Filtering gene expression correlation matrix in R
updated 3.0 years ago by 44k • written 10.1 years ago by ★ 4.8k
2
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1
reply
12k
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Answer: Answer: Filtering gene expression correlation matrix in R
updated 3.0 years ago by 44k • written 10.1 years ago by ★ 4.8k
0
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2
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3.3k
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Comment: C: DEXSeq with cufflinks gtf file
10.1 years ago by Sam ★ 4.8k
4
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1
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14k
views
Answer: A: Tutorial (How to analyze) on Whole Exome sequencing. Common Errors. Best Practic
10.1 years ago by Sam ★ 4.8k
1
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1
reply
3.3k
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Answer: Answer: DEXSeq with cufflinks gtf file
updated 2.8 years ago by 44k • written 10.1 years ago by ★ 4.8k
3
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1
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20k
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Answer: Answer: What is the simple way to remove known batch effect from RNA-seq data ?
updated 2.8 years ago by 44k • written 10.1 years ago by ★ 4.8k
647 results • Page 12 of 13
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