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Comment: C: How To Cluster Data That Contains Minor Allele, Somatic And Germline Frequencies
12.1 years ago by Sean Davis 27k
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Answer: A: Converting Probe Ids To Entrez Ids
12.2 years ago by Sean Davis 27k
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23k
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Comment: C: Large File Transfers Of Ngs Data: Rsync / Bbcp / Unison / What?
12.2 years ago by Sean Davis 27k
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23k
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Comment: C: Large File Transfers Of Ngs Data: Rsync / Bbcp / Unison / What?
12.2 years ago by Sean Davis 27k
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1
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23k
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Comment: C: Large File Transfers Of Ngs Data: Rsync / Bbcp / Unison / What?
12.2 years ago by Sean Davis 27k
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5.4k
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Comment: C: Best Practices For Publication Of Mrna-Seq Data
12.2 years ago by Sean Davis 27k
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2
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10k
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Comment: C: Best Human Genome Reference File For Gatk?
12.2 years ago by Sean Davis 27k
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4.1k
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Comment: C: Is It Possible For A Gene To Have A Mutation At The Same Position In Both Cosmic
12.2 years ago by Sean Davis 27k
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5.6k
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Comment: C: How To Find Number Of Mapped Reads For A Series Of Windows
12.2 years ago by Sean Davis 27k
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5.6k
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Comment: C: How To Find Number Of Mapped Reads For A Series Of Windows
12.2 years ago by Sean Davis 27k
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1
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5.6k
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Comment: C: How To Find Number Of Mapped Reads For A Series Of Windows
12.2 years ago by Sean Davis 27k
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1
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3.6k
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Comment: C: Using Miso For Exon-Centric Inference: Combine Bam Files From Replicates?
12.2 years ago by Sean Davis 27k
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76k
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Answer: Answer: Converting Affymetrix Probes To Gene Ids
updated 3.0 years ago by 45k • written 12.2 years ago by 27k
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2
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5.4k
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Comment: C: Wgcna -Dilemma In Choosing Soft Threshold
12.2 years ago by Sean Davis 27k
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5.6k
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Answer: A: How To Find Number Of Mapped Reads For A Series Of Windows
12.2 years ago by Sean Davis 27k
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2.0k
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Comment: C: Selecting Urn/Universe For Hypergeometric Test
12.2 years ago by Sean Davis 27k
4
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4.8k
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Answer: A: What Module To Use To Integrate R In Python : Rpy Or Rpy2
12.2 years ago by Sean Davis 27k
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1
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10k
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Comment: C: Rnaseq Fpkm Quantile Normalization
12.3 years ago by Sean Davis 27k
4
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1
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4.5k
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Comment: C: Integrative Bioinformatics: How To Integrate My Queries?
12.3 years ago by Sean Davis 27k
2
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1
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10k
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Comment: C: How To Analyse Epigenetics Data Using Bioinformatics Tools?
12.3 years ago by Sean Davis 27k
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3.3k
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Answer: A: Associating Gc Content With Genomic Features
12.3 years ago by Sean Davis 27k
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10k
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Comment: C: How To Analyse Epigenetics Data Using Bioinformatics Tools?
12.3 years ago by Sean Davis 27k
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0
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10k
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Answer: A: How To Merge Two Microarrays Datasets?
12.3 years ago by Sean Davis 27k
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1
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4.6k
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Comment: C: Tuxedo Suite: When To Skip Cufflinks/Cuffmerge?
12.3 years ago by Sean Davis 27k
1
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1
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4.6k
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Answer: A: Tuxedo Suite: When To Skip Cufflinks/Cuffmerge?
12.3 years ago by Sean Davis 27k
3
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2
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6.0k
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Answer: A: Combine Two Affymetrix Datasets With Same Platform
12.3 years ago by Sean Davis 27k
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4.7k
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Comment: C: Whole Genome Sequencing: Bwa
12.3 years ago by Sean Davis 27k
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0
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3.8k
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Comment: C: How To Verify That A Subset Of Genes Will Cluster Together
12.3 years ago by Sean Davis 27k
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1
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3.8k
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Comment: C: How To Verify That A Subset Of Genes Will Cluster Together
12.4 years ago by Sean Davis 27k
4
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1
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5.7k
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Answer: A: Installing Ggbio
12.4 years ago by Sean Davis 27k
1
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0
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4.0k
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Answer: A: Getting Sequence Information From Ucsc Genome Browser
12.4 years ago by Sean Davis 27k
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3.1k
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Comment: C: Deal With High Dimensions And Low Number Of Examples Gene Expression Data
12.4 years ago by Sean Davis 27k
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1
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3.1k
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Comment: C: Deal With High Dimensions And Low Number Of Examples Gene Expression Data
12.4 years ago by Sean Davis 27k
0
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1
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3.1k
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Answer: A: Deal With High Dimensions And Low Number Of Examples Gene Expression Data
12.4 years ago by Sean Davis 27k
4
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1
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4.0k
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Answer: A: Gene Ontology - Why Is There The Same Gene Name, Same Go Id Occurring Multiple T
12.4 years ago by Sean Davis 27k
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2.7k
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Answer: A: Assigning Significance To Variants In Two Populations
12.4 years ago by Sean Davis 27k
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3.7k
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Answer: A: Converting Solexa Reads To Fastq And Identifying Mismatched Bases
12.4 years ago by Sean Davis 27k
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1
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4.4k
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Comment: C: Cuffmerge : Why It Didn'T Merge These Transcripts Into One ?
12.4 years ago by Sean Davis 27k
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0
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2.7k
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Comment: C: Vcf Files From 1000 Genomes For Pypgen
12.4 years ago by Sean Davis 27k
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2.7k
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Comment: C: Vcf Files From 1000 Genomes For Pypgen
12.4 years ago by Sean Davis 27k
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0
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4.8k
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Comment: C: Alternatives To Gatk Indelrealigner?
12.4 years ago by Sean Davis 27k
0
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1
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4.8k
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Answer: A: Alternatives To Gatk Indelrealigner?
12.4 years ago by Sean Davis 27k
0
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1
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3.5k
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Comment: C: Tool To Differentiate Whole Genome And Segmental Duplication
12.4 years ago by Sean Davis 27k
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1
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3.5k
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Comment: C: Tool To Differentiate Whole Genome And Segmental Duplication
12.4 years ago by Sean Davis 27k
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0
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3.7k
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Answer: A: Help Interfacing With Ucsc Annotations Using Mysql
12.4 years ago by Sean Davis 27k
1
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4.8k
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Answer: A: Count Vs Dispersion Plot
12.4 years ago by Sean Davis 27k
5
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1
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8.5k
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Answer: A: How Do You Decide When A Sequencing Run Is Too Bad To Have Reliable Information?
12.4 years ago by Sean Davis 27k
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5.2k
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Answer: A: What Figure You Make For Qc Of Whole Exome Sequencing Data
12.4 years ago by Sean Davis 27k
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1
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4.9k
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Comment: C: Parse Ncbi Eutils Xml To Csv
12.4 years ago by Sean Davis 27k
2
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1
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4.9k
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Answer: A: Parse Ncbi Eutils Xml To Csv
12.4 years ago by Sean Davis 27k
1,985 results • Page 24 of 40
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