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42k
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Comment: C: Get Rs Number Based On Position
14.5 years ago by lh3 33k
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21k
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Comment: C: Why Are Sam/Bam Files So Large?
14.5 years ago by lh3 33k
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21k
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Comment: C: Why Are Sam/Bam Files So Large?
14.5 years ago by lh3 33k
6
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1
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3.5k
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Answer: A: How Does One Describe All Differences Between Two Complete Chromosomes?
14.5 years ago by lh3 33k
8
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1
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7.9k
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Answer: A: From Compressed Bam To Fastq
14.5 years ago by lh3 33k
5
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2
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4.1k
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Answer: A: Macrogen Vs Complete Genomics
14.5 years ago by lh3 33k
5
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6.2k
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Answer: A: Defining Your Reference Genome From Ucsc For Human Ngs Studies
14.5 years ago by lh3 33k
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13k
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Comment: C: The Meaning Of Samtools Flagstat Output Of Illumina'S Bam File
14.5 years ago by lh3 33k
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13k
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Comment: C: The Meaning Of Samtools Flagstat Output Of Illumina'S Bam File
14.5 years ago by lh3 33k
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0
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13k
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Comment: C: The Meaning Of Samtools Flagstat Output Of Illumina'S Bam File
14.5 years ago by lh3 33k
2
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11k
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Comment: C: Simple Retrieval Of 1000 Genomes Maf Using Rsids
14.5 years ago by lh3 33k
2
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1
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3.5k
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Answer: A: Tools For Large Indels Discovery In Single-End Rna-Seq Reads
14.5 years ago by lh3 33k
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6.1k
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Comment: C: Confused By Wgsim Output
14.5 years ago by lh3 33k
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0
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17k
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Comment: C: How To Predict Pseudogenes In A Genome
14.5 years ago by lh3 33k
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9.2k
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Comment: C: Which Programs Are You Relying On For Solid Data Analysis?
14.5 years ago by lh3 33k
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9.2k
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Comment: C: Which Programs Are You Relying On For Solid Data Analysis?
14.5 years ago by lh3 33k
8
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2.8k
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Answer: A: How Do I Get The Reads That Correspond To A Particular Gene Of Interest
14.5 years ago by lh3 33k
10
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1
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7.7k
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Answer: Answer: Has Anyone Had Experience With Complete Genomics Sequencing And Data Analysis?
updated 4.6 years ago by 45k • written 14.5 years ago by 33k
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1
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7.7k
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Comment: C: What Do You Think Microsoft Biology Foundation?
14.5 years ago by lh3 33k
2
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0
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5.2k
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Answer: A: Bwa Aln For Snp/Indel Discovery With Paired End 100Bp Human Dna Reads
14.5 years ago by lh3 33k
0
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0
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5.2k
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Comment: C: Bwa Aln For Snp/Indel Discovery With Paired End 100Bp Human Dna Reads
14.5 years ago by lh3 33k
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0
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6.5k
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Comment: C: Snp Calling By Comparing Normal Rna-Seq Data With Disease
14.5 years ago by lh3 33k
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0
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6.5k
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Comment: C: Snp Calling By Comparing Normal Rna-Seq Data With Disease
14.5 years ago by lh3 33k
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4.0k
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Comment: C: New Short Read Aligner On The Block Wham
14.5 years ago by lh3 33k
7
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0
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4.0k
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Answer: A: New Short Read Aligner On The Block Wham
14.5 years ago by lh3 33k
1
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0
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5.4k
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Answer: A: Did Any Of You Observe Rna Editing Or Have Ideas About The Mechanism? Idea For A
14.5 years ago by lh3 33k
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0
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4.0k
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Comment: C: New Short Read Aligner On The Block Wham
14.5 years ago by lh3 33k
4
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0
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4.0k
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Comment: C: New Short Read Aligner On The Block Wham
14.5 years ago by lh3 33k
4
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0
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4.0k
views
Comment: C: New Short Read Aligner On The Block Wham
14.5 years ago by lh3 33k
5
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6
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9.9k
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Answer: A: What Is The Best Method For Aligning Two Genome Assemblies?
14.5 years ago by lh3 33k
0
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0
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10k
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Comment: C: How To Retrieve Gene Variations From Ensembl Using The Perl Api?
14.5 years ago by lh3 33k
0
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0
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6.3k
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Comment: C: Best Way To Calculate Variation/Snp Density In The Ensembl Database?
14.5 years ago by lh3 33k
0
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0
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9.1k
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Comment: C: Which Program Should I Test To Map Rnaseq Data? Did Anybody Tried Gsnap?
14.5 years ago by lh3 33k
3
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0
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18k
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Comment: C: Convert Illumina Reads To Sanger Score
14.5 years ago by lh3 33k
0
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0
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6.4k
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Comment: C: Whole-Exome Data Cleanup / Filtering
14.5 years ago by lh3 33k
3
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1
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18k
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Comment: C: Convert Illumina Reads To Sanger Score
14.5 years ago by lh3 33k
0
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0
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6.4k
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Comment: C: Whole-Exome Data Cleanup / Filtering
14.5 years ago by lh3 33k
0
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0
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6.4k
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Comment: C: Whole-Exome Data Cleanup / Filtering
14.5 years ago by lh3 33k
1
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0
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5.3k
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Comment: Comment: Deep Exome Sequencing And Alignment To Hg18 Or Hg19?
updated 4.6 years ago by 45k • written 14.6 years ago by 33k
3
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0
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129k
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Comment: C: Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
14.6 years ago by lh3 33k
1
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0
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129k
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Comment: C: Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
14.6 years ago by lh3 33k
1
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0
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20k
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Comment: C: What Is The Difference Between Samtools Mpileup And Pileup
14.6 years ago by lh3 33k
0
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0
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11k
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Comment: C: What'S The Best Generic Scripting Tool For Bioinformatics?
14.6 years ago by lh3 33k
0
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0
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11k
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Comment: C: What'S The Best Generic Scripting Tool For Bioinformatics?
14.6 years ago by lh3 33k
0
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0
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11k
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Comment: C: What'S The Best Generic Scripting Tool For Bioinformatics?
14.6 years ago by lh3 33k
0
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0
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11k
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Comment: C: What'S The Best Generic Scripting Tool For Bioinformatics?
14.6 years ago by lh3 33k
1
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0
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11k
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Comment: C: What'S The Best Generic Scripting Tool For Bioinformatics?
14.6 years ago by lh3 33k
0
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0
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3.3k
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Comment: C: Snp Association Next Gen Sequencing
14.6 years ago by lh3 33k
0
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0
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6.4k
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Comment: C: Fast Method To Detect Whether Snp Lies In Sequence Feature
14.6 years ago by lh3 33k
4
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0
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9.0k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
14.6 years ago by lh3 33k
1,458 results • Page 24 of 30
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