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Comment: C: Help! Gene Ontology Enrichment Analysis
8.3 years ago by cpad0112 21k
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0
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3.5k
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Comment: C: What is the HGVS notation for the Hemophilia A intron 22 inversion mutation?
8.3 years ago by cpad0112 21k
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1
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3.5k
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Answer: A: What is the HGVS notation for the Hemophilia A intron 22 inversion mutation?
8.3 years ago by cpad0112 21k
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0
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3.5k
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Answer: A: What is the HGVS notation for the Hemophilia A intron 22 inversion mutation?
8.4 years ago by cpad0112 21k
0
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0
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3.9k
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Answer: A: How can I extract base on specific loci from all reads overlapping that?
8.4 years ago by cpad0112 21k
1
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0
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10k
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Answer: A: Transcript Id conversion
8.4 years ago by cpad0112 21k
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0
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3.5k
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Answer: A: What is the HGVS notation for the Hemophilia A intron 22 inversion mutation?
8.4 years ago by cpad0112 21k
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0
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1.6k
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Answer: A: How to treat ExpressionSet file
8.4 years ago by cpad0112 21k
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1
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7.2k
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Comment: C: Error in RCircos.Validate.Genomic.Data
8.4 years ago by cpad0112 21k
1
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1
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7.2k
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Answer: A: Error in RCircos.Validate.Genomic.Data
8.4 years ago by cpad0112 21k
1
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0
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8.1k
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Comment: C: show vcf data in a table
8.4 years ago by cpad0112 21k
0
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1
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2.9k
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Comment: C: Parsing GATK Variant Tables with R
8.4 years ago by cpad0112 21k
2
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1
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1.4k
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Comment: C: commands for RNAseq data analysis and variation(snp)
8.4 years ago by cpad0112 21k
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1
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3.1k
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Comment: C: Slicing a vcf file to just a few thousand SNPs with PyVCF.
8.4 years ago by cpad0112 21k
1
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0
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2.3k
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Answer: A: BQSR on one sample vs. all samples in a run
8.5 years ago by cpad0112 21k
1
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1
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3.3k
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Comment: A: Low gene count assignment for ribo-depleted RNA-Seq data?
8.5 years ago by cpad0112 21k
0
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2
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3.8k
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Comment: Comment: Computational Biologist opportunity at a CRISPR/Cas9 Startup, Intellia Therapeut
updated 3.1 years ago by 45k • written 10.0 years ago by 21k
0
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1
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4.7k
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Comment: C: vcfutils.pl issue, all nnnnn in fastq file
10.0 years ago by cpad0112 21k
0
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2
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3.8k
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Answer: A: Computational Biologist opportunity at a CRISPR/Cas9 Startup, Intellia Therapeut
10.0 years ago by cpad0112 21k
0
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0
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1.8k
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Comment: Comment: Newbie, SNP to gene analysis question
updated 3.1 years ago by 45k • written 10.0 years ago by 21k
0
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1
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2.6k
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Answer: A: Concordance NGS and array genotypes
10.0 years ago by cpad0112 21k
0
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1
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1.8k
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Answer: A: Newbie, SNP to gene analysis question
10.0 years ago by cpad0112 21k
2
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0
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3.6k
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Answer: A: error in running R
10.0 years ago by cpad0112 21k
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0
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1.9k
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Comment: Comment: Error while running discoSNP
10.0 years ago by cpad0112 21k
0
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1
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2.6k
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Comment: C: Concrodance NGS and array genotypes
10.0 years ago by cpad0112 21k
0
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0
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7.4k
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Comment: C: How to convert Affymetrix SNP IDs to dbSNP rs SNP names
10.0 years ago by cpad0112 21k
0
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1
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7.4k
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Comment: A: How to convert Affymetrix SNP IDs to dbSNP rs SNP names
10.0 years ago by cpad0112 21k
2
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1
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3.3k
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Answer: A: Scientific Project Manager, Seven Bridges Genomics, Cambridge, MA, USA
10.0 years ago by cpad0112 21k
1
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0
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1.8k
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Answer: A: Hiring San Francisco- PhD level NGS Bioinformaticians
10.0 years ago by cpad0112 21k
0
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0
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4.1k
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Answer: Answer: Finding the TFs that regulate a set of genes
updated 3.1 years ago by 45k • written 10.0 years ago by 21k
2
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0
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2.1k
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Comment: A: no accepted_hits.bam generated
10.0 years ago by cpad0112 21k
0
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0
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3.1k
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Answer: Answer: Is it possible to get a merged fasta/fastq reads from a bam file?
updated 3.1 years ago by 45k • written 10.0 years ago by 21k
0
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0
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9.5k
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Answer: Answer: Proper Way To Map Rna-Seq Data Against A Single (Or Small) Number Of Genes
updated 3.1 years ago by 45k • written 10.0 years ago by 21k
1
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1
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5.6k
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Answer: Answer: How to annotate SNP variant records in a vcf file with IDs from a bed file?
updated 3.1 years ago by 45k • written 10.0 years ago by 21k
0
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1
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5.3k
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Answer: A: Single end or paired end for variant calling
10.0 years ago by cpad0112 21k
0
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0
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2.5k
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Comment: C: Bioinformatician - Analyse 'omics data to help find drugs for rare diseases, Cam
10.0 years ago by cpad0112 21k
0
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1
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2.5k
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Comment: C: Bioinformatician - Analyse 'omics data to help find drugs for rare diseases, Cam
10.0 years ago by cpad0112 21k
2
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1
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2.1k
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Comment: C: VCF file format
10.0 years ago by cpad0112 21k
0
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1
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14k
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Comment: C: Is there a way to find the percent similarity just like percent identity in BLAS
10.0 years ago by cpad0112 21k
0
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0
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2.6k
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Answer: A: Post tagging etiquette musings
10.0 years ago by cpad0112 21k
1
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1
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14k
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Answer: A: Is there a way to find the percent similarity just like percent identity in BLAS
10.0 years ago by cpad0112 21k
1
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1
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2.4k
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Answer: A: Protein-Protein interaction in the NFKB pathway tool for multi-entry
10.0 years ago by cpad0112 21k
1
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1
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4.3k
views
Answer: A: Just got back raw Affy Axiom SNP data from core lab, where do I start? (new lear
10.0 years ago by cpad0112 21k
0
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0
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2.6k
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Comment: C: Normalization of Affymetrix data
10.0 years ago by cpad0112 21k
0
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1
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2.6k
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Comment: C: Normalization of Affymetrix data
10.0 years ago by cpad0112 21k
1
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0
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7.4k
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Answer: Answer: Thrown Into A Bioinformatics Position
updated 4.5 years ago by 45k • written 10.0 years ago by 21k
1
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0
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1.9k
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Answer: A: How to find biological meaning of my results at probe level ?
10.0 years ago by cpad0112 21k
0
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1
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2.6k
views
Answer: A: Normalization of Affymetrix data
10.0 years ago by cpad0112 21k
0
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1
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3.7k
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Answer: A: Affy Mouse Transcriptome Array analysis with Bioconductor
10.0 years ago by cpad0112 21k
2
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1
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6.0k
views
Comment: C: GenomicFeatures makeTxDbFromGFF: Select by columns in gtf file
10.0 years ago by cpad0112 21k
3,458 results • Page 68 of 70
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