cnv.chop.edu

Copy Number Variation

Chr 4 copy number variation frequency. High-resolution mapping of copy number variations in 2,026 healthy individuals. The OpenHelix Blog featured the CHOP CNV web site as the tip of the week. On November 4, 2009. Make sure to view the blog entry's video tutorial. The CNV project at CHOP is described in the manuscript High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Published by Genome Research.

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Copy Number Variation | cnv.chop.edu Reviews

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Chr 4 copy number variation frequency. High-resolution mapping of copy number variations in 2,026 healthy individuals. The OpenHelix Blog featured the CHOP CNV web site as the tip of the week. On November 4, 2009. Make sure to view the blog entry's video tutorial. The CNV project at CHOP is described in the manuscript High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Published by Genome Research.

<META> KEYWORDS

1 review and tutorial

2 please report

3 cnv query

4 position

5 gene offset

6 variation type

7 heterozygous deletion

8 homozygous deletion

9 duplication

10 uniqueness

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review and tutorial,please report,cnv query,position,gene offset,variation type,heterozygous deletion,homozygous deletion,duplication,uniqueness,non unique blue,unique green,more options,fewer options,ethnicity,african,european,asian,size bp,of snps,size

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Copy Number Variation | cnv.chop.edu Reviews

https://cnv.chop.edu

Chr 4 copy number variation frequency. High-resolution mapping of copy number variations in 2,026 healthy individuals. The OpenHelix Blog featured the CHOP CNV web site as the tip of the week. On November 4, 2009. Make sure to view the blog entry's video tutorial. The CNV project at CHOP is described in the manuscript High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Published by Genome Research.

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cnv.chop.edu

1

Copy Number Variation

http://cnv.chop.edu/;jsessionid=790D5A8AE3330442EE8015E8FA741E40

Chr 13 copy number variation frequency. High-resolution mapping of copy number variations in 2,026 healthy individuals. The OpenHelix Blog featured the CHOP CNV web site as the tip of the week. On November 4, 2009. Make sure to view the blog entry's video tutorial. The CNV project at CHOP is described in the manuscript High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Published by Genome Research.

2

Help - Copy Number Variation

http://cnv.chop.edu/help.jsp;jsessionid=790D5A8AE3330442EE8015E8FA741E40?sec=cnv_query

The methods used to detect the copy number variations served by this web site are described in the manuscript High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Published by Genome Research. CNV (Copy Number Variant). A frequency is attached to each CNV block, representing the percentage of study samples (individuals) that share this particular block. The user may search the CNV database for the three different copy ...

3

Acknowledgements - Copy Number Variation

http://cnv.chop.edu/acknowledgements.jsp;jsessionid=790D5A8AE3330442EE8015E8FA741E40

The authors of the CNV resource at Children's Hospital of Philadelphia (CHOP) would like to thank the individuals who donated blood samples for the genotyping data. We are very thankful for the valuable input and feedback from the CHOP Stokes research community over the months. We would also like to express our appreciation toward the Hospital and the Joseph Stokes Jr. Research Institute for providing resources and the opportunity to participate in such an important and exciting research project.

4

Help - Copy Number Variation

http://cnv.chop.edu/help.jsp;jsessionid=790D5A8AE3330442EE8015E8FA741E40?sec=position

The methods used to detect the copy number variations served by this web site are described in the manuscript High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Published by Genome Research. CNV (Copy Number Variant). A frequency is attached to each CNV block, representing the percentage of study samples (individuals) that share this particular block. The user may search the CNV database for the three different copy ...

5

Downloads - Copy Number Variation

http://cnv.chop.edu/data_downloads.jsp;jsessionid=790D5A8AE3330442EE8015E8FA741E40

CHOP normals (annotation updated Apr 28, 2010; data unchanged as of Jul 10, 2009 manuscript). CHOP CNV dataset of 2,026 healthy individuals. MySQL database dumps of the CHOP CNV data (primarily for CNV Workshop). Demo data for CNV Workshop. CNV Workshop CentOS VM images. CHOP CNV dataset of 2,026 healthy individuals. Selected tables in tab-delimited format, in hg17 coordinates. Lifted-over hg18 coordinates are available in a MySQL database dump (below). For advanced users only. Cnv2 h17.mysqldump&#46...

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Applications - Department of Biomedical and Health Informatics

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Harvest Program: Integrated Research Databases. Care Assistant Program: EHR Prompts, Interventions, and Decision Support. Asthma Clinical Decision Support. Research Recruitment Prompts in Primary Care. REDCap Program: User-Enabled Data Management. Proband- Pedigrees Made Simple. Mobile Health Application Development Program. Clinical Trial Management Systems. Laboratory Information Management Systems. The Harvest Program: Integrated Research Databases. Dynamic querying engine with visualizations. The Car...

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cnv.chop.edu

Copy Number Variation

Chr 4 copy number variation frequency. High-resolution mapping of copy number variations in 2,026 healthy individuals. The OpenHelix Blog featured the CHOP CNV web site as the tip of the week. On November 4, 2009. Make sure to view the blog entry's video tutorial. The CNV project at CHOP is described in the manuscript High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Published by Genome Research.

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