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Answer: Answer: Somatic variant calling mutect2 ctDNA liquid biopsy
12 months ago by tomas4482 ▴ 400
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468
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Answer: Answer: How can I make a similar mutated gene expression figure with TCGA data
13 months ago by tomas4482 ▴ 400
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1.1k
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Answer: Answer: Seurat Metadata to Dataframe Manipulation
14 months ago by tomas4482 ▴ 400
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520
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Answer: Answer: Batch effect removal for RNA-seq data (single-end and pair-end)
19 months ago by tomas4482 ▴ 400
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465
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Answer: Answer: RNA-seq data from human patients with both GBM and Alzheimer's
20 months ago by tomas4482 ▴ 400
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1.2k
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Answer: Answer: Variant identified, What next?
20 months ago by tomas4482 ▴ 400
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1.1k
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Answer: Answer: Merging different fastq files into one folder
21 months ago by tomas4482 ▴ 400
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2.8k
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Answer: Answer: How to convert a FASTQ file to FASTA file without the number of reads
21 months ago by tomas4482 ▴ 400
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2.6k
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Answer: Answer: Installing ensembl-vep
21 months ago by tomas4482 ▴ 400
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484
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Answer: Answer: How to match tumor fastq file to normal fastq file? (I just have a set of tumor
21 months ago by tomas4482 ▴ 400
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1.1k
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Answer: Answer: merging data; remove extra rows
21 months ago by tomas4482 ▴ 400
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Answer: Answer: Retrieval of specific classes from an Ontology
21 months ago by tomas4482 ▴ 400
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2.3k
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Answer: Answer: SRA not splitting when trying to download fastq
21 months ago by tomas4482 ▴ 400
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951
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Answer: Answer: correlation among RNAseq and proteomics analysis
21 months ago by tomas4482 ▴ 400
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3.5k
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Answer: Answer: Distinguish between forward strand, plus strand, sense strand
21 months ago by tomas4482 ▴ 400
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1.1k
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Answer: Answer: The nightmare of coordinate systems
22 months ago by tomas4482 ▴ 400
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814
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Answer: Answer: Make a specific format gene ontology file?
22 months ago by tomas4482 ▴ 400
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2.3k
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Answer: Answer: Downloading a huge amount of Fastq files
22 months ago by tomas4482 ▴ 400
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488
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Answer: Answer: Why does the CADD database have multiple lines for the same mutation/substitutio
22 months ago by tomas4482 ▴ 400
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704
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Answer: Answer: Get nucleotide sequence of assembled RNA transcripts
22 months ago by tomas4482 ▴ 400
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1.9k
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Answer: Answer: how can we count that how many alignments contains a deletion?please guide me
23 months ago by tomas4482 ▴ 400
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Answer: Answer: Colon cancer and single nucleotide variants
23 months ago by tomas4482 ▴ 400
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3.8k
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Answer: Answer: STAR alignment getting KILLED in process. Please help!
23 months ago by tomas4482 ▴ 400
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1.2k
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Answer: Answer: Why after normalization of scRNA-Seq data by DESeq2 the p-value of a large numbe
23 months ago by tomas4482 ▴ 400
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948
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Answer: Answer: Seurat dotplot
2.1 years ago by tomas4482 ▴ 400
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649
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Answer: Answer: Does anyone know how to use Human Splicing Finder?
2.1 years ago by tomas4482 ▴ 400
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712
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Answer: Answer: Help with adding new ID names to read count
2.1 years ago by tomas4482 ▴ 400
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2.8k
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Answer: Answer: BAM file reads mapping to multiple genes
2.5 years ago by tomas4482 ▴ 400
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2.4k
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Answer: Answer: featureCounts has low successfully assigned reads
2.6 years ago by tomas4482 ▴ 400
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3.1k
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Answer: Answer: Base recalibration in normal vs. tumor somatic variant calling in WXS data?
2.6 years ago by tomas4482 ▴ 400
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3.8k
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Answer: Answer: Aspera: Failed to authenticate
2.6 years ago by tomas4482 ▴ 400
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1.6k
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Answer: Answer: SRA/ENA library layout is inconsistent with the data source
2.7 years ago by tomas4482 ▴ 400
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872
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Answer: Answer: Single-cell RNA Seq on whole organ or whole tissue with known cell origins
2.7 years ago by tomas4482 ▴ 400
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