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Answer:
Answer: Reading microarray data from the Gene Expression Omnibus
2.6 years ago by
Kevin Blighe
87k
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1.0k
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Answer:
Answer: ROC_AUC curve for performance of a classification
2.6 years ago by
Kevin Blighe
87k
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3.0k
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Answer: Haploview and plink
2.6 years ago by
Kevin Blighe
87k
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736
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Answer: Disease Causing Mutations Databases or database for predicting the functional co
2.6 years ago by
Kevin Blighe
87k
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966
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Answer:
Answer: where do I find transcript_biotype
2.7 years ago by
Kevin Blighe
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3.0k
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Answer: Need help to remove NA values from data frame
2.7 years ago by
Kevin Blighe
87k
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1.0k
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Answer:
Answer: snp analysis
2.7 years ago by
Kevin Blighe
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815
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Answer: qPCR data analysis
2.7 years ago by
Kevin Blighe
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645
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Answer:
Answer: SNPs Datasets
2.7 years ago by
Kevin Blighe
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Answer: how to build an interaction network in R
2.7 years ago by
Kevin Blighe
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Answer:
Answer: bcftools multiallelic split not working
2.7 years ago by
Kevin Blighe
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Answer: WGCNA for diferent stages (I-IV)
2.7 years ago by
Kevin Blighe
87k
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3.3k
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Answer: pre-proccessing of RNAseq data for WGCNA
2.7 years ago by
Kevin Blighe
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Answer: Problems with downloading fastq files from sra-toolkit
2.7 years ago by
Kevin Blighe
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6.8k
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Answer: How to change the default font in ggplot 2
2.7 years ago by
Kevin Blighe
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1.4k
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Answer:
Answer: bash script
2.7 years ago by
Kevin Blighe
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927
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Answer:
Answer: VEP output is only protein_coding
2.7 years ago by
Kevin Blighe
87k
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893
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Answer:
Answer: problem in y axis in barplot+ggplot
2.7 years ago by
Kevin Blighe
87k
2
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1.7k
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Answer:
Answer: r is running out of memory
2.7 years ago by
Kevin Blighe
87k
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Answer:
Answer: Validation of somatic variant calling pipeline
2.7 years ago by
Kevin Blighe
87k
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1.6k
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Answer:
Answer: [HuGene-1_0-st] Affymetrix Human Gene 1.0 ST Array [transcript (gene) version],
2.7 years ago by
Kevin Blighe
87k
0
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1.4k
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Answer:
Answer: microarray miRNA expression data analysis
2.8 years ago by
Kevin Blighe
87k
1
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2.4k
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Answer:
Answer: Bioperl SeqIO.pm cannot be found
2.8 years ago by
Kevin Blighe
87k
3
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1.5k
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Answer:
Answer: AnnotationHub::mapIds() cannot find existing ENSG (GEO supplemental data cross-r
2.8 years ago by
Kevin Blighe
87k
0
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871
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Answer:
Answer: Extremely low number of variants in VCF file after filtering MIN(FORMAT/DP)>10
2.8 years ago by
Kevin Blighe
87k
1
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811
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Answer:
Answer: How to perform DESEQ2 analysis when there are three treatments (one of them bein
2.8 years ago by
Kevin Blighe
87k
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1.7k
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Answer:
Answer: How to compare LD of a gene for all subpopulations in 1000 Genome?
2.8 years ago by
Kevin Blighe
87k
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1.5k
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Answer:
Answer: R package for filtering expression data
2.8 years ago by
Kevin Blighe
87k
0
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4.4k
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Answer:
Answer: K-means for RNA seq gene clustering
2.8 years ago by
Kevin Blighe
87k
1
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1.4k
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Answer:
Answer: Paired-end to Single-end
2.8 years ago by
Kevin Blighe
87k
1
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5.1k
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Answer:
Answer: inquiry related to snpsift
2.8 years ago by
Kevin Blighe
87k
2
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1.6k
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Answer:
Answer: What is the best annotation tool?
2.8 years ago by
Kevin Blighe
87k
1
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951
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Answer:
Answer: Forum: Job opportunities in Europe, with and without a PhD
2.8 years ago by
Kevin Blighe
87k
4
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1
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2.8k
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Answer:
Answer: Displaying points which fall outside of the plot window in EnhancedVolcano
2.8 years ago by
Kevin Blighe
87k
0
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0
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1.2k
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Answer:
Answer: variant calling
2.8 years ago by
Kevin Blighe
87k
2
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2
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5.4k
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Answer:
Answer: Bcftools how to add DP to FORMAT field (get per sample read depth for REF vs AL
2.8 years ago by
Kevin Blighe
87k
2
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0
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621
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Answer:
Answer: why is important to identify genetic risk variants?
2.8 years ago by
Kevin Blighe
87k
1
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703
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Answer:
Answer: P value signficancy
updated 15 months ago by
Ram
43k • written 2.8 years ago by
Kevin Blighe
87k
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1.4k
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Answer:
Answer: Ensembl encoding problem
2.8 years ago by
Kevin Blighe
87k
0
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1.7k
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Answer:
Answer: Batch correction proteomics dataset
2.8 years ago by
Kevin Blighe
87k
3
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1
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854
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Answer:
Answer: DESeq2: impact of number of expressed genes in differential expression analysis
2.8 years ago by
Kevin Blighe
87k
2
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1.1k
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Answer:
Answer: separate multi-alleles from bi-alleles
2.8 years ago by
Kevin Blighe
87k
0
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0
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615
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Answer:
Answer: Copy number alteration prediction from DNA-seq
2.8 years ago by
Kevin Blighe
87k
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1.8k
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Answer:
Answer: Query for limma and DEseq2
2.8 years ago by
Kevin Blighe
87k
0
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1.4k
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Answer:
Answer: fgsea gene names
2.8 years ago by
Kevin Blighe
87k
4
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1
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1.2k
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Answer:
Answer: How to normalize and transform RNA-seq data of different samples for PCA?
2.8 years ago by
Kevin Blighe
87k
0
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1
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1.6k
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Answer:
Answer: Manhattan plot p-value
2.9 years ago by
Kevin Blighe
87k
2
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1
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1.6k
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Answer:
Answer: How to convert genotypes "1, 2" to "0,1, 2"?
2.9 years ago by
Kevin Blighe
87k
0
votes
0
replies
791
views
Answer:
Answer: Help with processing GSE63060: Illumina data that does not have lumi requirement
2.9 years ago by
Kevin Blighe
87k
2
votes
0
replies
790
views
Answer:
Answer: Suggestions for an undergraduate research project on glioblastoma
2.9 years ago by
Kevin Blighe
87k
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