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Answer: A: How To Remove The Identifier And Quality From A Fastq File
updated 4.7 years ago by 45k • written 12.3 years ago by 3.5k
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Answer: A: What is the convention for CNV vcf output in chromosome X and Y?
updated 5.2 years ago by 45k • written 10.8 years ago by 3.5k
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Answer: A: analysis of Homozygosity mapping
updated 5.2 years ago by 45k • written 10.8 years ago by 3.5k
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1
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3.2k
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Answer: A: Constructing Enzyme Network
updated 5.3 years ago by 45k • written 12.6 years ago by 3.5k
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3.1k
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Comment: C: Assumptions About Snps?
updated 5.3 years ago by 45k • written 13.0 years ago by 3.5k
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37k
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Comment: C: How Can I Calculate The Depth Of The Sequencing?
updated 5.3 years ago by 45k • written 13.1 years ago by 3.5k
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Answer: A: Calculating Sequencing Depth Of A Genomic Region
updated 5.5 years ago by 45k • written 11.0 years ago by 3.5k
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14k
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Comment: C: Gatk Multi-Sample Calling
updated 5.5 years ago by 45k • written 13.0 years ago by 3.5k
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Comment: C: Best Free Text Editor For All Popular Languages (R, Python, Perl Etc..)
updated 5.5 years ago by 45k • written 13.1 years ago by 3.5k
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Answer: A: Why Do We Need Markduplicates For Variants Detection In Gatk Processing Pipeline
updated 5.5 years ago by 45k • written 13.0 years ago by 3.5k
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2.3k
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Answer: A: Epigenetics
updated 6.5 years ago by 45k • written 12.9 years ago by 3.5k
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6
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9.9k
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Sources Of Publicly Available Human Whole Genome Sequence Data
next-gen data
updated 7.3 years ago by 20 • written 12.9 years ago by 3.5k
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0
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22k
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Comment: Comment: Large File Transfers Of Ngs Data: Rsync / Bbcp / Unison / What?
updated 2.3 years ago by 45k • written 9.8 years ago by 3.5k
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4.8k
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Answer: Answer: Mapping Variants to Protein Seqeunces
updated 3.0 years ago by 45k • written 10.2 years ago by 3.5k
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4.4k
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Answer: A: what is your daily must see bioinformatics web site?
10.6 years ago by Alex Paciorkowski 3.5k
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6.8k
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Answer: Answer: Help with Creating Gene Diagram for Research Article
updated 3.2 years ago by 45k • written 10.6 years ago by 3.5k
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1
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34k
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Comment: Comment: Why are we still using Bam files? And not Cram, HDF5 or improved Bam files?
updated 4.0 years ago by 45k • written 10.6 years ago by 3.5k
1
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0
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4.2k
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Comment: Comment: Does CNVs are genetically inherited?
updated 3.3 years ago by 45k • written 10.6 years ago by 3.5k
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1
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3.0k
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Comment: C: Regarding GATK pipelie
10.6 years ago by Alex Paciorkowski 3.5k
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2.4k
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Comment: C: Web server to analyze sequence data
10.7 years ago by Alex Paciorkowski 3.5k
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2.8k
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Comment: C: Laboratoy Scientific - Biochemist
10.7 years ago by Alex Paciorkowski 3.5k
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3.0k
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Comment: C: CHI SQUARE TEST IN R for SPNs bacterial data
10.7 years ago by Alex Paciorkowski 3.5k
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4.1k
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Comment: C: analysis of Homozygosity mapping
10.8 years ago by Alex Paciorkowski 3.5k
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2.3k
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Answer: A: How to determine whether a secondary structure prediction is significant or rele
11.0 years ago by Alex Paciorkowski 3.5k
26
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9
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19k
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8 follow
Favorite Splice Site Prediction/Evaluation Tools
splicing prediction
updated 21 months ago by ▴ 30 • written 12.3 years ago by 3.5k
2
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0
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4.3k
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Answer: A: Companies Providing Exome Sequencing And/Or Dna Segment Sequencing?
updated 4.0 years ago by 45k • written 11.1 years ago by 3.5k
3
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0
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2.8k
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Answer: A: Confirming Identified Seq Mutations By Pcr
11.1 years ago by Alex Paciorkowski 3.5k
2
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0
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6.1k
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Comment: C: Filter Germline Mutations From .Vcf
11.1 years ago by Alex Paciorkowski 3.5k
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1
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2.8k
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Comment: C: Vcf Quality Double For Alternate Loci Vs Reference Loci
11.2 years ago by Alex Paciorkowski 3.5k
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1
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3.9k
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Answer: A: Data Of Sift And Polyphen
11.2 years ago by Alex Paciorkowski 3.5k
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1
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5.7k
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Comment: C: Pacbio Sequencing Reads Data Output
11.2 years ago by Alex Paciorkowski 3.5k
3
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7.5k
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Answer: A: How Do You Usually Filter Variant Calling Results?
11.2 years ago by Alex Paciorkowski 3.5k
2
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3
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2.9k
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Answer: A: Ten Recommendations For Creating Usable Bioinformatics Command Line Software
11.2 years ago by Alex Paciorkowski 3.5k
5
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2
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6.2k
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Analysis Of Short Tandem Repeats/Trinucleotides In Ngs Data -- Revisited
exome genome analysis
updated 11.2 years ago by 20 • written 11.6 years ago by 3.5k
1
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0
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3.9k
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Comment: C: Predict Effects Of Missense Mutations On Structure
11.3 years ago by Alex Paciorkowski 3.5k
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0
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5.9k
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Comment: C: What Next After Snp Identification
11.3 years ago by Alex Paciorkowski 3.5k
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1
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2.9k
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Comment: C: Rare Variants
11.3 years ago by Alex Paciorkowski 3.5k
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0
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7.3k
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Comment: C: Standard Post Variant Call (Vcf) Analysis That Work Out Of The Box
11.3 years ago by Alex Paciorkowski 3.5k
2
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0
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4.0k
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Answer: A: Information Has Missed And Messed After Converting Annotated Whole-Genome Data I
11.3 years ago by Alex Paciorkowski 3.5k
2
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0
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2.9k
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Answer: A: Indel Prioritizing Method To Extract Most Damaging Effect On Protein
11.3 years ago by Alex Paciorkowski 3.5k
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1
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17k
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Comment: C: Fda Sends A Warning Letter To 23Andme - Personal Genomics Service Marketing To B
11.3 years ago by Alex Paciorkowski 3.5k
3
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1
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20k
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Answer: A: Macosx For Bioinformatics?
11.3 years ago by Alex Paciorkowski 3.5k
2
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0
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20k
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Comment: C: Macosx For Bioinformatics?
11.3 years ago by Alex Paciorkowski 3.5k
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0
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2.7k
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Answer: A: Classify Proteins Into Classes
11.4 years ago by Alex Paciorkowski 3.5k
1
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1
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17k
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Comment: C: Sequencing Your Own Genome! How Can It Be Done? Has Anyone Here Done It?
11.5 years ago by Alex Paciorkowski 3.5k
1
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1
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7.6k
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Comment: Comment: How To Analyze Your Own Exome
updated 4.0 years ago by 45k • written 11.6 years ago by 3.5k
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0
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Answer: A: Gatk Mutli-Samples Vcf
11.6 years ago by Alex Paciorkowski 3.5k
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0
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6.6k
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Comment: C: Transcription Factors <--> Regulated Genes Database
11.6 years ago by Alex Paciorkowski 3.5k
0
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1
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7.6k
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Comment: Comment: How To Analyze Your Own Exome
updated 4.0 years ago by 45k • written 11.6 years ago by 3.5k
4
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0
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6.5k
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Answer: A: How Complex It Is To Analyze Ngs Data ?
11.6 years ago by Alex Paciorkowski 3.5k
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