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Comment: Comment: Extract nucleotide sequence from a RefSeq Transcript ID
3.2 years ago by LauferVA 4.8k
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Comment: Comment: Extract nucleotide sequence from a RefSeq Transcript ID
3.2 years ago by LauferVA 4.8k
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2.5k
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Comment: Comment: Extract nucleotide sequence from a RefSeq Transcript ID
3.2 years ago by LauferVA 4.8k
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Answer: Answer: Modelling vs removing effects from confounding variables and their uses for down
3.2 years ago by LauferVA 4.8k
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Comment: Comment: Extract nucleotide sequence from a RefSeq Transcript ID
3.2 years ago by LauferVA 4.8k
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2.5k
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Comment: Comment: Extract nucleotide sequence from a RefSeq Transcript ID
3.2 years ago by LauferVA 4.8k
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Finding Specific Types of Data for Cancer Studies
TCGA GDC Cancer Entrez GEO
3.2 years ago by LauferVA 4.8k
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Comment: Comment: Extract nucleotide sequence from a RefSeq Transcript ID
3.2 years ago by LauferVA 4.8k
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2.5k
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Extract nucleotide sequence from a RefSeq Transcript ID
nucleotide refseq transcript sequence entrez
3.2 years ago by LauferVA 4.8k
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Comment: Comment: How can I detect mutations that occur more than once in a location with PYTHON?
3.3 years ago by LauferVA 4.8k
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71k
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Comment: Comment: Docker denied: requested access to the resource is denied
3.3 years ago by LauferVA 4.8k
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Comment: Comment: Best resource for getting a person with a Math/Comp Sci background the right amo
3.3 years ago by LauferVA 4.8k
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Forum: Best resource for getting a person with a Math/Comp Sci background the right amount of Biology knowledge
biology teaching
updated 2.9 years ago by 45k • written 3.3 years ago by 4.8k
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3.1k
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Comment: Comment: Tips and tricks for using ImageJ
3.3 years ago by LauferVA 4.8k
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3.1k
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Tips and tricks for using ImageJ
imageJ macros automation
updated 3.3 years ago by ▴ 930 • written 3.3 years ago by 4.8k
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950
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Comment: Comment: Multi-allelic sites in Identity-by-descent tract detection
3.3 years ago by LauferVA 4.8k
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Comment: Comment: understanding ariant allele frequency for paired ended reads
3.4 years ago by LauferVA 4.8k
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3.1k
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Answer: Answer: Feature Selection in Large Dataset with High Multicollinearity
3.4 years ago by LauferVA 4.8k
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115k
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Answer: Answer: What Are The Most Common Stupid Mistakes In Bioinformatics?
3.4 years ago by LauferVA 4.8k
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837
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Comment: Comment: What does different columns for merged gtf file represents?
3.4 years ago by LauferVA 4.8k
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586
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Comment: Comment: Clustering GO
3.4 years ago by LauferVA 4.8k
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Comment: Comment: Comparing bed files for shifts and enlargements
3.4 years ago by LauferVA 4.8k
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Comment: Comment: About Whole Exome Sequencing analysis
3.4 years ago by LauferVA 4.8k
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4.9k
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Comment: Comment: hg19 interval list
3.4 years ago by LauferVA 4.8k
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Answer: Answer: Figures of gene ontology pathways
3.4 years ago by LauferVA 4.8k
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Comment: Comment: Batch correction for scRNAseq when wildtypes and mutants were sequenced in separ
3.4 years ago by LauferVA 4.8k
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2.3k
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Answer: Answer: Batch correction for scRNAseq when wildtypes and mutants were sequenced in separ
3.4 years ago by LauferVA 4.8k
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2.8k
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Comment: Comment: Ewing sarcoma "related" genes ?
3.4 years ago by LauferVA 4.8k
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1.1k
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Comment: Comment: somatic SNV tool for ONT samples
3.4 years ago by LauferVA 4.8k
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1.5k
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Comment: Comment: About Whole Exome Sequencing analysis
3.4 years ago by LauferVA 4.8k
2
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2.2k
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Comment: Comment: Extraction of high variance or contributing genes using pcatools
3.4 years ago by LauferVA 4.8k
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1.8k
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Comment: Comment: Comparative transcriptomics
3.4 years ago by LauferVA 4.8k
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1.3k
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Answer: Answer: Python script to process NGS data
3.4 years ago by LauferVA 4.8k
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1
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2.8k
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Answer: Answer: Ewing sarcoma "related" genes ?
3.4 years ago by LauferVA 4.8k
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2.3k
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Comment: Comment: Finding longest CDS for the sequence
3.4 years ago by LauferVA 4.8k
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889
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Answer: Answer: Should we include genotype as covariates when performing EWAS?
3.4 years ago by LauferVA 4.8k
1
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1
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949
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Comment: Comment: Need help in finding pseudo genes using python script
updated 2.9 years ago by 45k • written 3.4 years ago by 4.8k
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1
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1.4k
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Comment: Comment: Noob question: I want to use TCGA data to compare survival with mutations, how s
3.4 years ago by LauferVA 4.8k
1
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2
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1.4k
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Comment: Comment: Noob question: I want to use TCGA data to compare survival with mutations, how s
3.4 years ago by LauferVA 4.8k
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0
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1.2k
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Comment: Comment: locus discrepancy
3.4 years ago by LauferVA 4.8k
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1.2k
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Comment: Comment: locus discrepancy
3.4 years ago by LauferVA 4.8k
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1.4k
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Comment: Comment: PCA plot interpretation after accounting for batch effects with SVA
3.4 years ago by LauferVA 4.8k
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1.4k
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Comment: Comment: PCA plot interpretation after accounting for batch effects with SVA
3.4 years ago by LauferVA 4.8k
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0
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911
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Comment: Comment: Genes mutations in cancer
3.5 years ago by LauferVA 4.8k
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923
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Comment: Comment: Building A Ultrametric Phylogenetic Tree With Integer Branch Length
3.5 years ago by LauferVA 4.8k
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2.2k
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Answer: Answer: Accessing COSMIC database via Python script
3.5 years ago by LauferVA 4.8k
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1
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915
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Comment: Comment: Unique mutations between VCF files
3.5 years ago by LauferVA 4.8k
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850
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Answer: Answer: Reasonable number of mutations in a human cancer cell exome
3.5 years ago by LauferVA 4.8k
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0
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932
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Answer: Answer: 3 group differential gene analysis
3.5 years ago by LauferVA 4.8k
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1
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4.3k
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Comment: Comment: SQL-why do we need it in Bioinformatics ?
3.6 years ago by LauferVA 4.8k
793 results • Page 10 of 16
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