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3
votes
1
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3.2k
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Answer: C: Agilent single color array
6.1 years ago by andrew.j.skelton73 6.6k
1
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1
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1.3k
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Answer: A: Proxy variants by GRCh37 position
6.2 years ago by andrew.j.skelton73 6.6k
3
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0
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2.5k
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Answer: A: Differential Gene Expression between 2 RNA seq groups without normal control
6.2 years ago by andrew.j.skelton73 6.6k
1
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2
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11k
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Answer: A: How to overcome "duplicate row.names" error while importing tpm/count/fpkm matri
6.2 years ago by andrew.j.skelton73 6.6k
2
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0
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1.5k
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Answer: A: Is it normal a substantial reduction of BAM files after ordering ?
6.2 years ago by andrew.j.skelton73 6.6k
4
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1
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2.7k
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Answer: A: SNP calling in 2018
6.2 years ago by andrew.j.skelton73 6.6k
1
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0
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5.1k
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Answer: C: makeTxDbFromGFF Problem - GenomicFeatures R package
6.2 years ago by andrew.j.skelton73 6.6k
0
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1
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9.9k
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Answer: A: IGV command line control
6.2 years ago by andrew.j.skelton73 6.6k
2
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0
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1.4k
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Answer: A: QTL /linkage trait mapping
6.2 years ago by andrew.j.skelton73 6.6k
1
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2
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3.0k
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Answer: C: Base Recabiliration Filters out 88% of the reads
6.3 years ago by andrew.j.skelton73 6.6k
0
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0
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2.2k
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Answer: A: Cufflinks and StringTie
6.3 years ago by andrew.j.skelton73 6.6k
1
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1
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2.8k
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Answer: A: Getting files from BaseMount (Using find command to loop through the symlinks)
6.3 years ago by andrew.j.skelton73 6.6k
2
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0
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5.7k
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Answer: A: Using gVCF mode in HaplotypeCaller ( GATK4)
6.3 years ago by andrew.j.skelton73 6.6k
3
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0
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2.9k
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Answer: A: opensource grafical user interface for filtering millions of annotated variant
6.3 years ago by andrew.j.skelton73 6.6k
2
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1
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3.9k
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Answer: A: WES -- How come I found 40% mutations intron regions
6.4 years ago by andrew.j.skelton73 6.6k
7
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0
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4.8k
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Answer: A: What Are The Most Influential Bioinformatics/Computational Biology Papers Of 201
6.4 years ago by andrew.j.skelton73 6.6k
1
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0
replies
3.1k
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Answer: A: WES germline CNV caller for trio analysis
6.5 years ago by andrew.j.skelton73 6.6k
7
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1
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8.0k
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Answer: A: Alternatives to Venn Diagrams
6.5 years ago by andrew.j.skelton73 6.6k
1
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0
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1.1k
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Answer: A: Bayesian Estimation of Temporal Regulation-RNASeq
6.5 years ago by andrew.j.skelton73 6.6k
0
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0
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1.5k
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Answer: A: probe's p.value in 450 k array
6.6 years ago by andrew.j.skelton73 6.6k
1
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1
reply
3.2k
views
Answer: A: How to convert VCF file into a binary matrix to find the genotype markers
6.6 years ago by andrew.j.skelton73 6.6k
1
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2
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3.0k
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Answer: A: Infinium Methylation SNP
6.6 years ago by andrew.j.skelton73 6.6k
4
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1
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2.7k
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Answer: C: Problem with Ensembl version identifiers after running DESeq2
6.6 years ago by andrew.j.skelton73 6.6k
1
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1
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3.5k
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Answer: A: phasing variants to find de novos
6.6 years ago by andrew.j.skelton73 6.6k
0
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0
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2.5k
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Answer: A: Questions about truncated dummy BAM files, functionality of SAMTOOLS mpileup, an
6.6 years ago by andrew.j.skelton73 6.6k
2
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1
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2.1k
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Answer: A: Any coexpression tools for RNAseq expression data
6.6 years ago by andrew.j.skelton73 6.6k
0
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0
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1.6k
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Answer: A: Determine "global" methylation from Illumina EPIC data?
6.6 years ago by andrew.j.skelton73 6.6k
0
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0
replies
2.3k
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Answer: A: Model matrix for limma voom
6.6 years ago by andrew.j.skelton73 6.6k
3
votes
0
replies
3.1k
views
Answer: A: GATK; Variant calling RNA-Seq best practices: bam processing steps
6.6 years ago by andrew.j.skelton73 6.6k
3
votes
1
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5.7k
views
Answer: A: Taking out , vsd <- varianceStabilizingTransformation(dds) from deseq2
6.6 years ago by andrew.j.skelton73 6.6k
1
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1
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2.1k
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Answer: A: Cufflinks with large BAM file
6.6 years ago by andrew.j.skelton73 6.6k
4
votes
2
replies
2.3k
views
Answer: A: retrospective trio analysis from WGS SNPs
6.7 years ago by andrew.j.skelton73 6.6k
2
votes
1
reply
3.0k
views
Answer: A: vennDigram for multiple RNA-seq data
6.7 years ago by andrew.j.skelton73 6.6k
2
votes
0
replies
2.2k
views
Answer: A: Tophat Error Message
6.8 years ago by andrew.j.skelton73 6.6k
2
votes
2
replies
2.1k
views
Answer: A: RNA_seq analysis cuffdiff output
6.8 years ago by andrew.j.skelton73 6.6k
2
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0
replies
1.8k
views
Answer: A: independent component analysis of RNA seq data
6.8 years ago by andrew.j.skelton73 6.6k
2
votes
1
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3.0k
views
Answer: A: adjusting p-value for GO analysis
6.8 years ago by andrew.j.skelton73 6.6k
1
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0
replies
2.2k
views
Answer: A: Is GATK overestimating the heterozygous calls?
6.8 years ago by andrew.j.skelton73 6.6k
0
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1
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2.9k
views
Answer: A: RNAseq variant filtering criteria
6.8 years ago by andrew.j.skelton73 6.6k
2
votes
1
reply
2.5k
views
Answer: A: Cis- eQTL Question
6.8 years ago by andrew.j.skelton73 6.6k
1
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1
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1.4k
views
Answer: A: CUfflink data for statistical test
6.8 years ago by andrew.j.skelton73 6.6k
2
votes
1
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7.5k
views
Answer: A: Kallisto pseudobam to IGV
6.8 years ago by andrew.j.skelton73 6.6k
2
votes
1
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2.5k
views
Answer: C: GATK variantFiltration unexpected behaviour?
6.8 years ago by andrew.j.skelton73 6.6k
3
votes
0
replies
2.3k
views
Answer: A: Transcripts read count
6.9 years ago by andrew.j.skelton73 6.6k
2
votes
1
reply
3.0k
views
Answer: A: Kallisto : Compare TPM between samples from different illumina sequencers (HiSeq
6.9 years ago by andrew.j.skelton73 6.6k
4
votes
1
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3.0k
views
Answer: A: how to calling variants in RNAseq data from multiple samples?
6.9 years ago by andrew.j.skelton73 6.6k
2
votes
0
replies
2.4k
views
Answer: A: Best practises RNAseq - Sleuth vs. NA's in annotation
6.9 years ago by andrew.j.skelton73 6.6k
0
votes
0
replies
2.6k
views
Answer: A: Regarding GATK for snp analysis
6.9 years ago by andrew.j.skelton73 6.6k
1
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1
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2.6k
views
Answer: A: The same Illumina expression data gathered by GEOquery and direct download shows
6.9 years ago by andrew.j.skelton73 6.6k
1
vote
1
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2.1k
views
Answer: A: methylation probe numbers
6.9 years ago by andrew.j.skelton73 6.6k
280 results • Page 3 of 6
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