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Answer: A: question for Accession No. : SSR
7.3 years ago by andrew.j.skelton73 6.6k
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Answer: A: Question regarding Bioinformatics with R and large comparisons
7.3 years ago by andrew.j.skelton73 6.6k
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Comment: C: stringTie Warning message
7.3 years ago by andrew.j.skelton73 6.6k
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4.1k
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Answer: A: CNV calling using ExomeDepth
7.3 years ago by andrew.j.skelton73 6.6k
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2.9k
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Comment: C: Linkage analysis with whole -exome sequencing data
7.3 years ago by andrew.j.skelton73 6.6k
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Answer: A: Some explanation about what a paired-end sequencing really means
7.4 years ago by andrew.j.skelton73 6.6k
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3.1k
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Comment: C: retrospective trio analysis from WGS SNPs
7.4 years ago by andrew.j.skelton73 6.6k
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Answer: A: Removing batch effects between Affymetrix and Agilent platforms using ComBat
7.4 years ago by andrew.j.skelton73 6.6k
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Comment: C: Surrogate variable analysis: ask for a practical example
7.4 years ago by andrew.j.skelton73 6.6k
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Answer: A: Surrogate variable analysis: ask for a practical example
7.4 years ago by andrew.j.skelton73 6.6k
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Comment: C: Deseq2 batch effect design issue
7.4 years ago by andrew.j.skelton73 6.6k
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4.6k
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Comment: C: Deseq2 batch effect design issue
7.4 years ago by andrew.j.skelton73 6.6k
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Comment: C: Deseq2 batch effect design issue
7.4 years ago by andrew.j.skelton73 6.6k
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Answer: A: What are the requirements to use data generated in other microarray experiments
7.4 years ago by andrew.j.skelton73 6.6k
2
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Answer: A: Transcription Factor Network
7.4 years ago by andrew.j.skelton73 6.6k
2
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1
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2.8k
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Set Difference in VCF Files
vcf vcftools
updated 3.2 years ago by 45k • written 9.6 years ago by 6.6k
3
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1
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3.8k
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Answer: C: Agilent single color array
7.4 years ago by andrew.j.skelton73 6.6k
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1
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1.6k
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Answer: A: Proxy variants by GRCh37 position
7.5 years ago by andrew.j.skelton73 6.6k
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2.9k
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Answer: A: Differential Gene Expression between 2 RNA seq groups without normal control
7.5 years ago by andrew.j.skelton73 6.6k
1
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12k
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Comment: C: How to overcome "duplicate row.names" error while importing tpm/count/fpkm matri
7.5 years ago by andrew.j.skelton73 6.6k
1
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2
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12k
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Answer: A: How to overcome "duplicate row.names" error while importing tpm/count/fpkm matri
7.5 years ago by andrew.j.skelton73 6.6k
2
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2.2k
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Answer: A: Is it normal a substantial reduction of BAM files after ordering ?
7.5 years ago by andrew.j.skelton73 6.6k
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3.3k
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Comment: C: SNP calling in 2018
7.6 years ago by andrew.j.skelton73 6.6k
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3.3k
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Answer: A: SNP calling in 2018
7.6 years ago by andrew.j.skelton73 6.6k
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Answer: C: makeTxDbFromGFF Problem - GenomicFeatures R package
7.6 years ago by andrew.j.skelton73 6.6k
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1
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13k
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Answer: A: IGV command line control
7.6 years ago by andrew.j.skelton73 6.6k
2
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1.7k
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Answer: A: QTL /linkage trait mapping
7.6 years ago by andrew.j.skelton73 6.6k
1
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2
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3.8k
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Answer: C: Base Recabiliration Filters out 88% of the reads
7.6 years ago by andrew.j.skelton73 6.6k
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0
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2.5k
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Answer: A: Cufflinks and StringTie
7.6 years ago by andrew.j.skelton73 6.6k
1
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1
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2.2k
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Comment: C: diffrential expression analysis
7.6 years ago by andrew.j.skelton73 6.6k
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1
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3.8k
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Comment: C: Getting files from BaseMount (Using find command to loop through the symlinks)
7.6 years ago by andrew.j.skelton73 6.6k
1
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1
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3.8k
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Answer: A: Getting files from BaseMount (Using find command to loop through the symlinks)
7.6 years ago by andrew.j.skelton73 6.6k
2
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6.2k
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Answer: A: Using gVCF mode in HaplotypeCaller ( GATK4)
7.6 years ago by andrew.j.skelton73 6.6k
3
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3.6k
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Answer: A: opensource grafical user interface for filtering millions of annotated variant
7.6 years ago by andrew.j.skelton73 6.6k
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Comment: C: WES -- How come I found 40% mutations intron regions
7.8 years ago by andrew.j.skelton73 6.6k
0
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1
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4.9k
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Comment: C: WES -- How come I found 40% mutations intron regions
7.8 years ago by andrew.j.skelton73 6.6k
2
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1
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4.9k
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Answer: A: WES -- How come I found 40% mutations intron regions
7.8 years ago by andrew.j.skelton73 6.6k
7
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0
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5.9k
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Answer: A: What Are The Most Influential Bioinformatics/Computational Biology Papers Of 201
7.8 years ago by andrew.j.skelton73 6.6k
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Comment: C: Illumina Instrument Type from fastq?
7.8 years ago by andrew.j.skelton73 6.6k
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0
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44k
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Comment: C: Illumina Instrument Type from fastq?
7.8 years ago by andrew.j.skelton73 6.6k
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3.5k
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Answer: A: WES germline CNV caller for trio analysis
7.8 years ago by andrew.j.skelton73 6.6k
7
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1
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8.9k
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Answer: A: Alternatives to Venn Diagrams
7.8 years ago by andrew.j.skelton73 6.6k
21
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13
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6.9k
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12 follow
Forum: User Friendly VCF Filtering Tools
vcf variant-calling
updated 2.5 years ago by 45k • written 9.3 years ago by 6.6k
0
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0
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6.9k
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Comment: C: User Friendly VCF Filtering Tools
7.9 years ago by andrew.j.skelton73 6.6k
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5
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5.7k
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Transcription Factor Binding Sites
sequence-search TFBS
updated 3.5 years ago by 45k • written 10.8 years ago by 6.6k
1
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0
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1.4k
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Answer: A: Bayesian Estimation of Temporal Regulation-RNASeq
7.9 years ago by andrew.j.skelton73 6.6k
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1
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2.3k
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Comment: C: how to automate microarray data analysis
7.9 years ago by andrew.j.skelton73 6.6k
1
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0
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2.1k
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Comment: C: Error when run testForDEU DEXSeq
7.9 years ago by andrew.j.skelton73 6.6k
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0
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1.8k
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Answer: A: probe's p.value in 450 k array
7.9 years ago by andrew.j.skelton73 6.6k
1
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1
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3.8k
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Answer: A: How to convert VCF file into a binary matrix to find the genotype markers
7.9 years ago by andrew.j.skelton73 6.6k
702 results • Page 5 of 15
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