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952
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Comment: C: Cell ratio between FACS and 10X
3.4 years ago by igor 13k
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827
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Answer: A: <5 genes as markers for scRNA Cluster?
3.4 years ago by igor 13k
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1.1k
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interactive browser for single-cell RNA-seq data
scrna-seq
3.4 years ago by igor 13k
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4.0k
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Comment: C: Integrating two Seurat Objects
3.4 years ago by igor 13k
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806
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Comment: C: Pre-ranked GSEA on gene clusters
3.4 years ago by igor 13k
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4.0k
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Answer: A: Integrating two Seurat Objects
3.4 years ago by igor 13k
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3.4k
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Comment: C: GSVA / ssGSEA on single cell RNA cluster
3.4 years ago by igor 13k
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3.4k
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Comment: C: GSVA / ssGSEA on single cell RNA cluster
3.4 years ago by igor 13k
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1.1k
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Comment: C: Mutect2 missing mutations
3.4 years ago by igor 13k
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1.7k
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Answer: A: Estimation of Copy Number of alterations(CNA) in Sc-RNA Seq data
3.4 years ago by igor 13k
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923
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Comment: C: how to calculate TMB from call stats file
3.4 years ago by igor 13k
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2.1k
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Comment: C: Best practices to perform a gene set enrichment analysis (GSEA) with E. coli?
3.4 years ago by igor 13k
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2.1k
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Comment: C: Best practices to perform a gene set enrichment analysis (GSEA) with E. coli?
3.4 years ago by igor 13k
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624
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Answer: A: Do different cells transcribe different amounts of gene data?
3.4 years ago by igor 13k
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1
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2.1k
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Comment: C: Best practices to perform a gene set enrichment analysis (GSEA) with E. coli?
3.4 years ago by igor 13k
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710
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Answer: A: "Bias" in NGS sequencing processing
3.4 years ago by igor 13k
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1
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923
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Comment: C: how to calculate TMB from call stats file
3.4 years ago by igor 13k
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1
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1.1k
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Answer: A: GDC TCGA LUAD dataset iCluster.group parameter
3.4 years ago by igor 13k
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4.8k
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Comment: C: Timeline for hg39 human genome?
3.4 years ago by igor 13k
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1.0k
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Comment: C: Changing chromosome names in BAM files
3.4 years ago by igor 13k
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1.3k
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Comment: C: Is Bioinformatics enough? Is it taken seriously?
3.4 years ago by igor 13k
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2.9k
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Comment: C: Is first strand the sense or the antisense?
3.5 years ago by igor 13k
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785
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Comment: C: difference between genotyping and sequencing ?
3.5 years ago by igor 13k
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1.4k
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Comment: C: Mutation calling directly from FASTQ files
3.5 years ago by igor 13k
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1
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1.4k
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Comment: C: Mutation calling directly from FASTQ files
3.5 years ago by igor 13k
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1.6k
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Comment: C: Tools for hard trimming?
3.5 years ago by igor 13k
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4.8k
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Answer: A: RNAseq RSEM and featurecounts
3.5 years ago by igor 13k
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1
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1.6k
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Comment: C: Tools for hard trimming?
3.5 years ago by igor 13k
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1.6k
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Answer: A: Tools for hard trimming?
3.5 years ago by igor 13k
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726
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Comment: C: The need for matched normal in variant-calling: gene-panel vs. whole exome
3.5 years ago by igor 13k
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1
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1.3k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
3.5 years ago by igor 13k
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1
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1.3k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
3.5 years ago by igor 13k
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1
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1.3k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
3.5 years ago by igor 13k
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4.0k
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Comment: C: CellRanger with CITE-seq and hashing
3.5 years ago by igor 13k
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1
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1.3k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
3.5 years ago by igor 13k
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2.1k
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Comment: C: Why it is not use UMIs for RNA-seq?
3.5 years ago by igor 13k
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1.4k
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Comment: C: Any alternatives to Cellranger aligner that Seurat can read?
3.5 years ago by igor 13k
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1.2k
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Comment: C: Did TCGA consortium recommend any best practice guideline for cross-sample RNAse
3.5 years ago by igor 13k
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709
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Comment: C: LoFreq input file issues
3.5 years ago by igor 13k
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1
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4.3k
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Comment: C: Kraken2 Error in buildind NCBI bacterial database
3.6 years ago by igor 13k
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5.9k
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Comment: C: normalization in single cell RNAseq
3.6 years ago by igor 13k
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2
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36k
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Comment: C: How to embed known cell information into Seurat object? AddMetaData?
3.6 years ago by igor 13k
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1
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36k
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Comment: C: How to embed known cell information into Seurat object? AddMetaData?
3.6 years ago by igor 13k
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0
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1.4k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by igor 13k
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1
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1.4k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by igor 13k
1
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1
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1.4k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by igor 13k
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1
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1.4k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by igor 13k
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626
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Comment: C: How is 1000 genomes so accessible when many other genotype/sequencing projects a
3.7 years ago by igor 13k
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1.4k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
3.7 years ago by igor 13k
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0
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930
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Comment: C: Negative values HTSeq2
3.7 years ago by igor 13k
1,531 results • Page 3 of 31
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