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Answer:
Answer: Somatic variant calling mutect2 ctDNA liquid biopsy
10 months ago by
tomas4482
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427
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Answer:
Answer: How can I make a similar mutated gene expression figure with TCGA data
11 months ago by
tomas4482
▴ 390
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992
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Answer: Seurat Metadata to Dataframe Manipulation
13 months ago by
tomas4482
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489
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Answer: Batch effect removal for RNA-seq data (single-end and pair-end)
17 months ago by
tomas4482
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439
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Answer: RNA-seq data from human patients with both GBM and Alzheimer's
19 months ago by
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Answer:
Answer: Variant identified, What next?
19 months ago by
tomas4482
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1.0k
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Answer:
Answer: Merging different fastq files into one folder
19 months ago by
tomas4482
▴ 390
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2.6k
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Answer:
Answer: How to convert a FASTQ file to FASTA file without the number of reads
19 months ago by
tomas4482
▴ 390
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2.4k
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Answer: Installing ensembl-vep
19 months ago by
tomas4482
▴ 390
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456
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Answer:
Answer: How to match tumor fastq file to normal fastq file? (I just have a set of tumor
19 months ago by
tomas4482
▴ 390
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1.0k
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Answer:
Answer: merging data; remove extra rows
20 months ago by
tomas4482
▴ 390
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497
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Answer: Retrieval of specific classes from an Ontology
20 months ago by
tomas4482
▴ 390
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2.1k
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Answer:
Answer: SRA not splitting when trying to download fastq
20 months ago by
tomas4482
▴ 390
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894
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Answer:
Answer: correlation among RNAseq and proteomics analysis
20 months ago by
tomas4482
▴ 390
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3.2k
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Answer:
Answer: Distinguish between forward strand, plus strand, sense strand
20 months ago by
tomas4482
▴ 390
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1.1k
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Answer:
Answer: The nightmare of coordinate systems
21 months ago by
tomas4482
▴ 390
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750
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Answer:
Answer: Make a specific format gene ontology file?
21 months ago by
tomas4482
▴ 390
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2.1k
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Answer:
Answer: Downloading a huge amount of Fastq files
21 months ago by
tomas4482
▴ 390
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467
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Answer:
Answer: Why does the CADD database have multiple lines for the same mutation/substitutio
21 months ago by
tomas4482
▴ 390
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659
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Answer:
Answer: Get nucleotide sequence of assembled RNA transcripts
21 months ago by
tomas4482
▴ 390
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1.8k
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Answer:
Answer: how can we count that how many alignments contains a deletion?please guide me
21 months ago by
tomas4482
▴ 390
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371
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Answer:
Answer: Colon cancer and single nucleotide variants
21 months ago by
tomas4482
▴ 390
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3.5k
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Answer:
Answer: STAR alignment getting KILLED in process. Please help!
21 months ago by
tomas4482
▴ 390
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1.1k
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Answer:
Answer: Why after normalization of scRNA-Seq data by DESeq2 the p-value of a large numbe
21 months ago by
tomas4482
▴ 390
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909
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Answer:
Answer: Seurat dotplot
23 months ago by
tomas4482
▴ 390
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601
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Answer:
Answer: Does anyone know how to use Human Splicing Finder?
23 months ago by
tomas4482
▴ 390
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659
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Answer:
Answer: Help with adding new ID names to read count
24 months ago by
tomas4482
▴ 390
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2.6k
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Answer:
Answer: BAM file reads mapping to multiple genes
2.4 years ago by
tomas4482
▴ 390
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Answer:
Answer: featureCounts has low successfully assigned reads
2.4 years ago by
tomas4482
▴ 390
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2.9k
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Answer:
Answer: Base recalibration in normal vs. tumor somatic variant calling in WXS data?
2.4 years ago by
tomas4482
▴ 390
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3.6k
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Answer:
Answer: Aspera: Failed to authenticate
2.4 years ago by
tomas4482
▴ 390
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1.5k
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Answer:
Answer: SRA/ENA library layout is inconsistent with the data source
2.6 years ago by
tomas4482
▴ 390
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837
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Answer:
Answer: Single-cell RNA Seq on whole organ or whole tissue with known cell origins
2.6 years ago by
tomas4482
▴ 390
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