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Comment: C: Affy Data Into Illumina Genome Studio
updated 5.6 years ago by 45k • written 14.8 years ago by 5.0k
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Comment: C: Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
updated 6.5 years ago by 45k • written 14.7 years ago by 5.0k
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Comment: C: Is Clinvar the most comprehensive and reliable source of disease-causing genes a
6.6 years ago by Biomed 5.0k
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Comment: C: What are the resources to design the most comprehensive clinical SNP chip?
8.8 years ago by Biomed 5.0k
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2.6k
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Comment: C: How can design the most comprehensive "clinical" SNP chip?
8.8 years ago by Biomed 5.0k
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Comment: C: Conservation At Amino Acid Level
12.7 years ago by Biomed 5.0k
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4.6k
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Comment: C: Conservation At Amino Acid Level
12.7 years ago by Biomed 5.0k
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6.6k
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Comment: C: I Need To Plot 73 Mutations On A Large Gene With >60 Exons
12.8 years ago by Biomed 5.0k
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5.8k
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Comment: C: Which Mappability Track To Use?
13.1 years ago by Biomed 5.0k
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66k
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Comment: C: What Is The Difference Between Hg18 And Hg19?
13.1 years ago by Biomed 5.0k
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5.8k
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Comment: C: Which Mappability Track To Use?
13.1 years ago by Biomed 5.0k
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66k
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Comment: C: What Is The Difference Between Hg18 And Hg19?
13.1 years ago by Biomed 5.0k
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4.4k
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Comment: C: Bwa Aln For Snp/Indel Discovery With Paired End 100Bp Human Dna Reads
13.2 years ago by Biomed 5.0k
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Comment: C: Illlumina Paired End Reads File Format
13.2 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Il
13.3 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Il
13.3 years ago by Biomed 5.0k
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7.1k
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Comment: Comment: Human Variation Databases
updated 3.9 years ago by 45k • written 13.5 years ago by 5.0k
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Comment: C: Assembly For Rare Variants
13.5 years ago by Biomed 5.0k
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Comment: C: Assembly For Rare Variants
13.5 years ago by Biomed 5.0k
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4.8k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
13.7 years ago by Biomed 5.0k
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4.8k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
13.7 years ago by Biomed 5.0k
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5.2k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
13.7 years ago by Biomed 5.0k
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5.2k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
13.7 years ago by Biomed 5.0k
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4.0k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
13.7 years ago by Biomed 5.0k
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4.0k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
13.7 years ago by Biomed 5.0k
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4.8k
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Comment: C: Pysam Snp Calling
13.8 years ago by Biomed 5.0k
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4.8k
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Comment: C: Pysam Snp Calling
13.8 years ago by Biomed 5.0k
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4.8k
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Comment: C: Pysam Snp Calling
13.8 years ago by Biomed 5.0k
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3.6k
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Comment: C: Macrogen Vs Complete Genomics
13.8 years ago by Biomed 5.0k
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3.6k
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Comment: C: Macrogen Vs Complete Genomics
13.8 years ago by Biomed 5.0k
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5.2k
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Comment: C: Chr_Random Positions
13.9 years ago by Biomed 5.0k
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5.2k
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Comment: C: Chr_Random Positions
13.9 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.9 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.9 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.9 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.9 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.9 years ago by Biomed 5.0k
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8.0k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.9 years ago by Biomed 5.0k
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1
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31k
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Comment: C: Human Exome Capture Library Coordinates Download
13.9 years ago by Biomed 5.0k
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7.4k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
14.0 years ago by Biomed 5.0k
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7.4k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
14.0 years ago by Biomed 5.0k
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2.8k
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Comment: C: Non Uniform Gene Coverage And Cufflinks Predictions : Artifacts ?
14.0 years ago by Biomed 5.0k
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6.8k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
14.1 years ago by Biomed 5.0k
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6.8k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
14.1 years ago by Biomed 5.0k
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3.2k
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Comment: C: Snp Position Problem
14.1 years ago by Biomed 5.0k
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258k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
14.1 years ago by Biomed 5.0k
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258k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
14.1 years ago by Biomed 5.0k
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1
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258k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
14.1 years ago by Biomed 5.0k
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0
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31k
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Comment: C: Human Exome Capture Library Coordinates Download
14.1 years ago by Biomed 5.0k
0
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0
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258k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
14.1 years ago by Biomed 5.0k
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