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Comment: C: Affy Data Into Illumina Genome Studio
updated 4.1 years ago by 40k • written 13.4 years ago by 4.9k
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Comment: C: Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
updated 5.0 years ago by 40k • written 13.2 years ago by 4.9k
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Comment: C: Is Clinvar the most comprehensive and reliable source of disease-causing genes a
5.2 years ago by Biomed 4.9k
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Comment: C: What are the resources to design the most comprehensive clinical SNP chip?
7.3 years ago by Biomed 4.9k
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Comment: C: How can design the most comprehensive "clinical" SNP chip?
7.3 years ago by Biomed 4.9k
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Comment: C: Conservation At Amino Acid Level
11.2 years ago by Biomed 4.9k
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3.9k
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Comment: C: Conservation At Amino Acid Level
11.2 years ago by Biomed 4.9k
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Comment: C: I Need To Plot 73 Mutations On A Large Gene With >60 Exons
11.4 years ago by Biomed 4.9k
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Comment: C: Which Mappability Track To Use?
11.6 years ago by Biomed 4.9k
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61k
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Comment: C: What Is The Difference Between Hg18 And Hg19?
11.6 years ago by Biomed 4.9k
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4.7k
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Comment: C: Which Mappability Track To Use?
11.6 years ago by Biomed 4.9k
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61k
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Comment: C: What Is The Difference Between Hg18 And Hg19?
11.6 years ago by Biomed 4.9k
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3.7k
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Comment: C: Bwa Aln For Snp/Indel Discovery With Paired End 100Bp Human Dna Reads
11.7 years ago by Biomed 4.9k
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Comment: C: Illlumina Paired End Reads File Format
11.7 years ago by Biomed 4.9k
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Comment: C: Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Il
11.8 years ago by Biomed 4.9k
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Comment: C: Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Il
11.8 years ago by Biomed 4.9k
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Comment: Comment: Human Variation Databases
updated 2.5 years ago by 40k • written 12.0 years ago by 4.9k
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Comment: C: Assembly For Rare Variants
12.0 years ago by Biomed 4.9k
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Comment: C: Assembly For Rare Variants
12.0 years ago by Biomed 4.9k
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4.0k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
12.2 years ago by Biomed 4.9k
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4.0k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
12.2 years ago by Biomed 4.9k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
12.2 years ago by Biomed 4.9k
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4.5k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
12.2 years ago by Biomed 4.9k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
12.3 years ago by Biomed 4.9k
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3.3k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
12.3 years ago by Biomed 4.9k
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4.1k
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Comment: C: Pysam Snp Calling
12.3 years ago by Biomed 4.9k
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Comment: C: Pysam Snp Calling
12.3 years ago by Biomed 4.9k
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4.1k
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Comment: C: Pysam Snp Calling
12.3 years ago by Biomed 4.9k
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2.9k
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Comment: C: Macrogen Vs Complete Genomics
12.3 years ago by Biomed 4.9k
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2.9k
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Comment: C: Macrogen Vs Complete Genomics
12.3 years ago by Biomed 4.9k
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Comment: C: Chr_Random Positions
12.4 years ago by Biomed 4.9k
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Comment: C: Chr_Random Positions
12.4 years ago by Biomed 4.9k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
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1
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29k
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Comment: C: Human Exome Capture Library Coordinates Download
12.4 years ago by Biomed 4.9k
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5.6k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
12.5 years ago by Biomed 4.9k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
12.5 years ago by Biomed 4.9k
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Comment: C: Non Uniform Gene Coverage And Cufflinks Predictions : Artifacts ?
12.5 years ago by Biomed 4.9k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
12.6 years ago by Biomed 4.9k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
12.6 years ago by Biomed 4.9k
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2.9k
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Comment: C: Snp Position Problem
12.6 years ago by Biomed 4.9k
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226k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
12.7 years ago by Biomed 4.9k
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226k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
12.7 years ago by Biomed 4.9k
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1
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226k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
12.7 years ago by Biomed 4.9k
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29k
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Comment: C: Human Exome Capture Library Coordinates Download
12.7 years ago by Biomed 4.9k
0
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0
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226k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
12.7 years ago by Biomed 4.9k
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