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1.1k
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Comment: C: Cell ratio between FACS and 10X
4.0 years ago by igor 13k
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940
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Answer: A: <5 genes as markers for scRNA Cluster?
4.0 years ago by igor 13k
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1
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1.2k
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interactive browser for single-cell RNA-seq data
scrna-seq
4.0 years ago by igor 13k
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4.4k
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Comment: C: Integrating two Seurat Objects
4.0 years ago by igor 13k
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891
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Comment: C: Pre-ranked GSEA on gene clusters
4.0 years ago by igor 13k
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1
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4.4k
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Answer: A: Integrating two Seurat Objects
4.0 years ago by igor 13k
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3.8k
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Comment: C: GSVA / ssGSEA on single cell RNA cluster
4.0 years ago by igor 13k
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1
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3.8k
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Comment: C: GSVA / ssGSEA on single cell RNA cluster
4.0 years ago by igor 13k
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1.2k
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Comment: C: Mutect2 missing mutations
4.0 years ago by igor 13k
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2.0k
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Answer: A: Estimation of Copy Number of alterations(CNA) in Sc-RNA Seq data
4.0 years ago by igor 13k
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1.1k
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Comment: C: how to calculate TMB from call stats file
4.0 years ago by igor 13k
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2.5k
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Comment: C: Best practices to perform a gene set enrichment analysis (GSEA) with E. coli?
4.0 years ago by igor 13k
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1
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2.5k
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Comment: C: Best practices to perform a gene set enrichment analysis (GSEA) with E. coli?
4.0 years ago by igor 13k
1
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0
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687
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Answer: A: Do different cells transcribe different amounts of gene data?
4.0 years ago by igor 13k
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1
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2.5k
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Comment: C: Best practices to perform a gene set enrichment analysis (GSEA) with E. coli?
4.0 years ago by igor 13k
2
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0
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808
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Answer: A: "Bias" in NGS sequencing processing
4.0 years ago by igor 13k
0
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1
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1.1k
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Comment: C: how to calculate TMB from call stats file
4.0 years ago by igor 13k
1
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1
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1.3k
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Answer: A: GDC TCGA LUAD dataset iCluster.group parameter
4.0 years ago by igor 13k
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5.4k
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Comment: C: Timeline for hg39 human genome?
4.0 years ago by igor 13k
1
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0
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1.2k
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Comment: C: Changing chromosome names in BAM files
4.0 years ago by igor 13k
1
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1.6k
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Comment: C: Is Bioinformatics enough? Is it taken seriously?
4.0 years ago by igor 13k
1
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3.3k
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Comment: C: Is first strand the sense or the antisense?
4.0 years ago by igor 13k
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895
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Comment: C: difference between genotyping and sequencing ?
4.0 years ago by igor 13k
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0
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1.6k
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Comment: C: Mutation calling directly from FASTQ files
4.0 years ago by igor 13k
1
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1
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1.6k
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Comment: C: Mutation calling directly from FASTQ files
4.0 years ago by igor 13k
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1.9k
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Comment: C: Tools for hard trimming?
4.0 years ago by igor 13k
2
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5.6k
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Answer: A: RNAseq RSEM and featurecounts
4.0 years ago by igor 13k
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1
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1.9k
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Comment: C: Tools for hard trimming?
4.0 years ago by igor 13k
1
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0
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1.9k
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Answer: A: Tools for hard trimming?
4.0 years ago by igor 13k
1
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0
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799
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Comment: C: The need for matched normal in variant-calling: gene-panel vs. whole exome
4.0 years ago by igor 13k
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1
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1.6k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
4.0 years ago by igor 13k
2
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1
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1.6k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
4.0 years ago by igor 13k
1
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1
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1.6k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
4.0 years ago by igor 13k
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4.4k
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Comment: C: CellRanger with CITE-seq and hashing
4.0 years ago by igor 13k
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1
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1.6k
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Comment: C: is it meaningful to enrich an organism using ontology from a different organism?
4.0 years ago by igor 13k
1
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0
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3.0k
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Comment: C: Why it is not use UMIs for RNA-seq?
4.1 years ago by igor 13k
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0
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1.6k
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Comment: C: Any alternatives to Cellranger aligner that Seurat can read?
4.1 years ago by igor 13k
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1.4k
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Comment: C: Did TCGA consortium recommend any best practice guideline for cross-sample RNAse
4.1 years ago by igor 13k
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0
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772
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Comment: C: LoFreq input file issues
4.1 years ago by igor 13k
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1
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4.6k
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Comment: C: Kraken2 Error in buildind NCBI bacterial database
4.1 years ago by igor 13k
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0
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6.4k
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Comment: C: normalization in single cell RNAseq
4.2 years ago by igor 13k
1
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2
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39k
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Comment: C: How to embed known cell information into Seurat object? AddMetaData?
4.2 years ago by igor 13k
1
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1
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39k
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Comment: C: How to embed known cell information into Seurat object? AddMetaData?
4.2 years ago by igor 13k
1
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0
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1.6k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
4.2 years ago by igor 13k
0
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1
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1.6k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
4.2 years ago by igor 13k
1
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1
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1.6k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
4.2 years ago by igor 13k
0
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1
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1.6k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
4.2 years ago by igor 13k
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0
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713
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Comment: C: How is 1000 genomes so accessible when many other genotype/sequencing projects a
4.2 years ago by igor 13k
1
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1
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1.6k
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Comment: C: Somatic SNVs vs. Germline SNPs for allele-specific copy number analysis
4.2 years ago by igor 13k
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0
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1.1k
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Comment: C: Negative values HTSeq2
4.2 years ago by igor 13k
1,531 results • Page 3 of 31
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