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Answer: A: Wgs Coverage
10.7 years ago by William ★ 5.3k
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7.0k
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Answer: A: Extracting Information From Vcf File About Heterozygous,Homozygous From Gatk Pip
10.7 years ago by William ★ 5.3k
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10k
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Answer: A: Trinity Transcriptome Assembly
10.7 years ago by William ★ 5.3k
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3.7k
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Answer: A: Library To Parse Absolute Reference Positions Of Indels From A Bam Cigar String
10.7 years ago by William ★ 5.3k
4
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17k
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Answer: A: Gatk - Haplotypecaller Is So Slow, What Is Faster And As Good?
10.7 years ago by William ★ 5.3k
5
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239k
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Answer: A: Tools To Calculate Average Coverage For A Bam File?
10.7 years ago by William ★ 5.3k
3
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25k
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Answer: A: Calculate Coverage From Bam File
10.7 years ago by William ★ 5.3k
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4.4k
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Answer: A: How To Calculate Genotype Concordance Between Indel Call Sets?
10.8 years ago by William ★ 5.3k
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5.3k
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Answer: A: How To Select The Top 30% Variants (Based On Quality) From A Vcf File?
10.8 years ago by William ★ 5.3k
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5.3k
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Answer: A: What Are The It Requirements For High Throughput Sequence Analysis
10.8 years ago by William ★ 5.3k
7
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44k
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Answer: A: What'S The Meaning Of "Bridge Pcr" In The Next Generation Sequencing
10.8 years ago by William ★ 5.3k
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2
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14k
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Answer: A: Extract Coverage Track From Bam To Bed File
10.8 years ago by William ★ 5.3k
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5.3k
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Answer: A: How To Call Snp And Indel Based On A Sanger Sequences Based Bac Contig Vs Refere
10.9 years ago by William ★ 5.3k
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3.0k
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Answer: A: Workflow For Using Unified Genotyper For Bioscope Aligned Solid Targeted Capture
10.9 years ago by William ★ 5.3k
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3.5k
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Answer: A: Vcf Library/Parser That Lets You Add New Entries, Fields, Etc
11.0 years ago by William ★ 5.3k
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3.8k
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Answer: A: Tools For Quality Trimming Of Solid Reads In Colorspace.
11.0 years ago by William ★ 5.3k
3
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7.3k
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Answer: A: How Do You Decide When A Sequencing Run Is Too Bad To Have Reliable Information?
11.0 years ago by William ★ 5.3k
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5.3k
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Answer: A: How To Set Validation_Stringency In The Picard Api Directly From Java
11.0 years ago by William ★ 5.3k
5
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4.6k
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Answer: A: How To Get The Flanking Sequence Of A Set Of Snp Positions (From Ensembl?)
11.1 years ago by William ★ 5.3k
3
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1
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9.5k
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Answer: A: Question : Plotting Per Chromosome/All Chromosome Coverage From Ngs Bam File
11.1 years ago by William ★ 5.3k
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4.6k
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Answer: A: Removing Pcr Duplicates From Bam Without Collapsing Sequences By Position?
11.1 years ago by William ★ 5.3k
5
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4.9k
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Answer: A: What Approach Would You Recommend For Large Indel Detection With Solid Data
11.1 years ago by William ★ 5.3k
2
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1
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4.8k
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Answer: A: What Is The Proper Way To Think About Reinventing The Wheel As A Bioinformaticia
11.2 years ago by William ★ 5.3k
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7.0k
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Answer: A: Solid Sequencing Protocol And How To Obtain Quality Of Solid Reads?
11.2 years ago by William ★ 5.3k
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20k
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Answer: A: Best Copy Number Variation Tools
11.3 years ago by William ★ 5.3k
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4.7k
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Answer: A: How To Select A Private Snp With Gatk From A Multisample Vcf File
11.3 years ago by William ★ 5.3k
4
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1
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5.5k
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Answer: A: Where/How To Assess Which Bioinformatics Tools/Databases Are Most Used/Accessed?
11.3 years ago by William ★ 5.3k
2
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0
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1.8k
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Answer: A: Comparison Of Mappers With Features And Numbers Of Citations
11.3 years ago by William ★ 5.3k
2
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27k
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Answer: A: Data Too Big To Be Stored In Memory: Common Options
11.4 years ago by William ★ 5.3k
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2.9k
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Answer: A: Best Hardware Solution For Microsecond Molecular Dynamics
11.6 years ago by William ★ 5.3k
5
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15k
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Answer: A: Best Genome Browser To Look At Structural Variation Calls
updated 11.7 years ago by 19k • written 11.7 years ago by ★ 5.3k
81 results • Page 2 of 2
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