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A Deep Catalog of Human Genetic Variation. Thursday November 06, 2014. Phase3 variant calls for chrY are available, variant calls for chrX have been updated. Our final release of the Phase 3 variant set is now available on the. Including a newly added VCF file for chrY. The chrY variant calls were made with a different process from that of the autosomes; a separate README is available in the release directory describing some details. The VCF files in the main release directory are also now available here.

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A Deep Catalog of Human Genetic Variation. Thursday November 06, 2014. Phase3 variant calls for chrY are available, variant calls for chrX have been updated. Our final release of the Phase 3 variant set is now available on the. Including a newly added VCF file for chrY. The chrY variant calls were made with a different process from that of the autosomes; a separate README is available in the release directory describing some details. The VCF files in the main release directory are also now available here.

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Home | 1000 Genomes | 1000genomes.org Reviews

https://1000genomes.org

A Deep Catalog of Human Genetic Variation. Thursday November 06, 2014. Phase3 variant calls for chrY are available, variant calls for chrX have been updated. Our final release of the Phase 3 variant set is now available on the. Including a newly added VCF file for chrY. The chrY variant calls were made with a different process from that of the autosomes; a separate README is available in the release directory describing some details. The VCF files in the main release directory are also now available here.

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1000genomes.org

1

Variant Call Format | 1000 Genomes

http://www.1000genomes.org/wiki/Analysis/variant-call-format

IGSR: The International Genome Sample Resource. Providing ongoing support for the 1000 Genomes Project data. IGSR Sample Collection Principles. 1000 Genomes Project Publications. The VCF/BCF specification is no longer maintained by the 1000 Genomes Project. The group leading the management and expansion of the format is the Global Alliance for Genomics and Health Data Working group file format team. The main version of the specification can be found on https:/ github.com/samtools/hts-specs.

2

Which reference assembly do you use? | 1000 Genomes

http://www.1000genomes.org/faq/which-reference-assembly-do-you-use

IGSR: The International Genome Sample Resource. Providing ongoing support for the 1000 Genomes Project data. IGSR Sample Collection Principles. 1000 Genomes Project Publications. Which reference assembly do you use? The reference assembly the 1000 Genomes Project has mapped sequence data to has changed over the course of the project. For the pilot phase we mapped data to NCBI36. A copy of our reference fasta file can be found on the ftp site. How are your alignments generated? Site maintained by EMBL-EBI.

3

Variant Call Format | 1000 Genomes

http://www.1000genomes.org/wiki/analysis/variant%20call%20format/vcf-variant-call-format-version-41

IGSR: The International Genome Sample Resource. Providing ongoing support for the 1000 Genomes Project data. IGSR Sample Collection Principles. 1000 Genomes Project Publications. The VCF/BCF specification is no longer maintained by the 1000 Genomes Project. The group leading the management and expansion of the format is the Global Alliance for Genomics and Health Data Working group file format team. The main version of the specification can be found on https:/ github.com/samtools/hts-specs.

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opendataideajam.cyberport.hk

Open Data IdeaJam 2015 Workshop | Cyberport

http://opendataideajam.cyberport.hk/others.html

List of References on Open Data. The following information is only part of the open data sources available for the event and participants are free to use other data sources available in the market and their own datasets. Summary of Sample Datasets. Centaline Property Agency Limited. Last 30 days Mid-West Unit Transaction Records. Mid-West Private Residence List. Mid-West Online Listing Information. Parking In The West End. Legislative History of Bills. 2011 Population Census - Main Tabless. It is an idea...

uygboston2016.uygsymposium.com

FAQ | UYG Boston

http://uygboston2016.uygsymposium.com/faq

Press enter to begin your search. What is the goal of UYG? The goal of the UYG symposium is to facilitate the adoption of clinical whole-genome sequencing as a means to advance human health, through responsible, target educational outreach. As an attendee, you will not only experience a highly relevant, deeply personal, and richly educational program, but you will also be a part of an exciting movement that is pioneering the application of genomics-based healthcare into mainstream clinical practice.

gastroenterology.blueprintgenetics.com

Genetic testing for Pancreatitis - Gastroenterology

http://gastroenterology.blueprintgenetics.com/panels/pancreatitis-panel

Blueprint Genetics - Gastroenterology. Ear Nose and Throat. Whole Genome Del/Dup (CNV). Our Sequence Analysis is based on a proprietary targeted sequencing method OS-Seq and offers panels targeted for genes associated with certain phenotypes. A standard way to analyze NGS data for finding the genetic cause for Mendelian disorders. Results in 21 days. Targeted Del/Dup (CNV) analysis is used to detect bigger disease causing deletions or duplications from the disease-associated genes. Results in 21 days.

nature.com

A map of human genome variation from population-scale sequencing : Nature : Nature Research

http://www.nature.com/nature/journal/v467/n7319/full/nature09534.html

Jump to main content. International weekly journal of science. Structural biology: A peep through anion channels. Homologue structure of the SLAC1 anion channel for closing stomata in leaves. A map of human genome variation from population-scale sequencing. The 1000 Genomes Project Consortium. View interactive PDF in ReadCube. Data generation, alignment and variant discovery. Power to detect variants. Application to association studies. Mutation, recombination and natural selection. The number of variant...

ncbi.nlm.nih.gov

All Resources - Site Guide - NCBI

https://www.ncbi.nlm.nih.gov/Database

Skip to main content. All Chemicals and Bioassays Resources. BLAST (Basic Local Alignment Search Tool). Sequence Read Archive (SRA). All DNA and RNA Resources. BLAST (Basic Local Alignment Search Tool). Conserved Domain Search Service (CD Search). Vector Alignment Search Tool (VAST). All Data and Software Resources. Conserved Domain Database (CDD). Conserved Domain Search Service (CD Search). Structure (Molecular Modeling Database). Vector Alignment Search Tool (VAST). All Domains and Structures Resources.

bioinfolab.miamioh.edu

Liang Lab

http://bioinfolab.miamioh.edu/bioinfolab/databasesExt.php

Access scientific knowledge, and make your research visible. Connecting Research and Researchers. Citation-based Database ( Chun Liang. Biology and Biotech News. Major Bioinformatics Web Portals. The Arabidopsis Information Resource. The Elements of Bioinformatics. Salk Arabidopsis 1001 genomes. Genomics Analysis in the Cloud. Solve puzzles for science.

essentialmedgen.com

essentialmedgen

http://www.essentialmedgen.com/Nov--2012:-1000-Genomes-Project.php

Links to databases and analysis tools. Directories of gene testing labs. Genome browsers and scientific information re genes and proteins. Tools for DNA and protein sequence analysis. Websites useful when designing primers. Analysis of functional signficance of missense mutations. Human Genome Project: ethics and education. Updates and additional information. How "silent" mutations may not be silent. Fragile X premutations: pathogenic mechanism. Nov 2012: 1000 Genomes Project. Q009 Tumour suppressor genes.

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The Kim Tribe

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Main Page - Bio.pe.kr

From Bio.pe.kr. Retrieved from " http:/ www.1000genome.org/index.php/Main Page. Related Links [ Edit. This page was last modified on 23 March 2015, at 07:29. This page has been accessed 593,544 times. Content is available under BioLicense: the freest license. About Bio.pe.kr.

1000genomes.org

Home | 1000 Genomes

A Deep Catalog of Human Genetic Variation. Thursday November 06, 2014. Phase3 variant calls for chrY are available, variant calls for chrX have been updated. Our final release of the Phase 3 variant set is now available on the. Including a newly added VCF file for chrY. The chrY variant calls were made with a different process from that of the autosomes; a separate README is available in the release directory describing some details. The VCF files in the main release directory are also now available here.

1000genomics.com

Main Page - Bio.pe.kr

From Bio.pe.kr. Retrieved from " http:/ www.1000genomics.com/index.php/Main Page. Related Links [ Edit. This page was last modified on 23 March 2015, at 07:29. This page has been accessed 593,548 times. Content is available under BioLicense: the freest license. About Bio.pe.kr.

1000genomics.org

Main Page - Bio.pe.kr

From Bio.pe.kr. Retrieved from " http:/ www.1000genomics.org/index.php/Main Page. Related Links [ Edit. This page was last modified on 23 March 2015, at 07:29. This page has been accessed 593,545 times. Content is available under BioLicense: the freest license. About Bio.pe.kr.

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1000 Genres. | Reviewing Music Daily Through The Assignation Of Superfluous Genres.

Reviewing Music Daily Through The Assignation Of Superfluous Genres. August 20, 2013. 8220;Lettsanity” by Lettuce, off. This song is so goddamned funky I had to end a multi-year hiatus from this blog just to share it. Can you just imagine shimmying your way around a glitterfied version of the Full House set and having your womanizing friend with the coiff smash through a wall right as the horns peak at the 4:30 mark? From → 2012. July 8, 2011. 8220;Feel Me Flow” by Naughty By Nature, off. From → 1995.

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