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Answer: A: Novel Sequence Insertions 1000 Genomes Project
updated 3.7 years ago by 39k • written 9.1 years ago by ★ 1.8k
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2.5k
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Answer: Answer: Benefit of platinum genomes in WGS experiment
updated 14 months ago by 39k • written 8.4 years ago by ★ 1.8k
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2
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4.3k
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Answer: A: bam file assembly (1000 genomes)
8.6 years ago by zam.iqbal.genome ★ 1.8k
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1
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4.0k
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Answer: A: Variant Discovery In Bacteria
9.2 years ago by zam.iqbal.genome ★ 1.8k
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1
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5.2k
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Answer: A: Fasta Sequence For Each Hla Alleles
9.2 years ago by zam.iqbal.genome ★ 1.8k
4
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1
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3.8k
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Answer: A: Are There Population-Specific Snps Included In The 1000Genomes Vcf Files?
9.2 years ago by zam.iqbal.genome ★ 1.8k
4
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1
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7.8k
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Answer: A: Population-Scaled Recombination Rate
9.3 years ago by zam.iqbal.genome ★ 1.8k
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1
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5.4k
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Answer: A: How To Extract Core Genome From Whole Genome Sequence Data?
9.4 years ago by zam.iqbal.genome ★ 1.8k
7
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1
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3.2k
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Answer: A: Why Insertion Are Hard To Find By The Alignments Of Reads Than Deletion ?
9.4 years ago by zam.iqbal.genome ★ 1.8k
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1
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2.4k
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Answer: A: Programming Challenge: Quickest Way To Determine The "Superpopulation" From A Vc
9.4 years ago by zam.iqbal.genome ★ 1.8k
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1
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2.1k
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Answer: A: 1000 Variant Calling Parameters
9.4 years ago by zam.iqbal.genome ★ 1.8k
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3
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2.2k
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Answer: A: Fast And Accurate Method To Identify Genes In Whole Genome
9.5 years ago by zam.iqbal.genome ★ 1.8k
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0
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4.3k
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Answer: A: Very Large Insertion Detection Methodology Query
9.6 years ago by zam.iqbal.genome ★ 1.8k
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1
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2.8k
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Answer: A: Snp Marker Development Using Rad Sequencing
9.6 years ago by zam.iqbal.genome ★ 1.8k
3
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1
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3.2k
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Answer: A: Most Appropriate Software Detect Population Specific Structural Variation In Mul
9.8 years ago by zam.iqbal.genome ★ 1.8k
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3
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16k
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Answer: A: Gatk - Haplotypecaller Is So Slow, What Is Faster And As Good?
9.8 years ago by zam.iqbal.genome ★ 1.8k
2
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10k
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Answer: A: Downstream Analysis
9.9 years ago by zam.iqbal.genome ★ 1.8k
13
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0
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16k
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Answer: Answer: Advice For Newcomers To The Bioinformatics Field
updated 6 months ago by 39k • written 9.9 years ago by ★ 1.8k
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0
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5.0k
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Answer: A: How To Call Snp And Indel Based On A Sanger Sequences Based Bac Contig Vs Refere
10.0 years ago by zam.iqbal.genome ★ 1.8k
2
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1
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8.4k
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Answer: A: Transition/Transversion Ratio From Fastq Files
10.0 years ago by zam.iqbal.genome ★ 1.8k
34
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1
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16k
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Answer: A: Decoy In Reference Assembly
10.0 years ago by zam.iqbal.genome ★ 1.8k
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1
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2.0k
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Answer: A: A Map(?) Of Sequence Alignment
10.0 years ago by zam.iqbal.genome ★ 1.8k
3
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0
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2.3k
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Answer: A: Retrieving Individual Genomes From 1000Genomes Project
10.2 years ago by zam.iqbal.genome ★ 1.8k
1
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0
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1.9k
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Answer: A: Reduced Represented Lib - Snp Calling In Unaligned Regions.
10.2 years ago by zam.iqbal.genome ★ 1.8k
2
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3
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6.0k
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Answer: A: Tool Recommendations For Human Genome Assembly
10.3 years ago by zam.iqbal.genome ★ 1.8k
4
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1
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3.7k
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Answer: A: Tools For Combined Genome Variation Analysis Of Short Sequencing Reads For Sever
updated 10.3 years ago by 98k • written 10.3 years ago by ★ 1.8k
2
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0
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4.4k
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Answer: A: Represent Precise Deletion In Vcf
10.3 years ago by zam.iqbal.genome ★ 1.8k
4
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0
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2.2k
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Answer: A: How To Generate Two Haplotypes Using Velvet
10.3 years ago by zam.iqbal.genome ★ 1.8k
18
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1
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40k
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Answer: A: How To Assess The Quality Of An Assembly? (Is There No Magic Formula?)
10.4 years ago by zam.iqbal.genome ★ 1.8k
2
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1
reply
12k
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Answer: A: Best Practice On Variant Discovery For Bacteria?
10.4 years ago by zam.iqbal.genome ★ 1.8k
2
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0
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2.8k
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Answer: A: Copy Number Variation For Haploid Organisms
10.5 years ago by zam.iqbal.genome ★ 1.8k
3
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1
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3.4k
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Answer: A: Insertion Detection Tools
10.7 years ago by zam.iqbal.genome ★ 1.8k
1
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0
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1.9k
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Answer: A: Subjects In 1000 Genome Removed In Recent Releases
10.7 years ago by zam.iqbal.genome ★ 1.8k
1
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1
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3.3k
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Answer: A: Best Existing Tool For Computing The Overlaps Between Each Read In A Set Of Shor
10.9 years ago by zam.iqbal.genome ★ 1.8k
4
votes
2
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10k
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Answer: A: Why Are There More Non-Synonymous Snps Than Synonymous Snps In The 1000 Genomes
10.9 years ago by zam.iqbal.genome ★ 1.8k
2
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2
replies
2.9k
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Answer: A: Trio: Detecting A Large De Novo Indel
11.0 years ago by zam.iqbal.genome ★ 1.8k
0
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0
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1.7k
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Answer: A: Statistical Model For Genotyping Based On Putative Structural Variants
11.0 years ago by zam.iqbal.genome ★ 1.8k
37 results • Page 1 of 1
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