Gerstein Lab Structural Variations

Portal for genome SV research in the Gerstein Lab. Personal genome constructor, it can be used to construct a personal diploid genome sequence by including personal variants into reference genome. A tool for CNV discovery and genotyping from depth of read mapping. A tools that implements an algorithm for optimal alignment of sequences with SVs. A pipeline for annotation, classification and analysis of SVs at single nucleotide resolution. Nat Biotechnol. 2010 Jan;28147-55. Epub 2009 Dec 27. Science46.

OVERVIEW

This web site sv.gersteinlab.org presently has a traffic classification of zero (the lower the better). We have audited six pages inside the web site sv.gersteinlab.org and found three websites interfacing with sv.gersteinlab.org.
Pages Analyzed
6
Links to this site
3

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This web site sv.gersteinlab.org is seeing fluctuating levels of traffic all over the year.
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WHAT DOES SV.GERSTEINLAB.ORG LOOK LIKE?

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SV.GERSTEINLAB.ORG HOST

Our web crawlers found that a lone root page on sv.gersteinlab.org took two hundred and sixty-six milliseconds to come up. We could not discover a SSL certificate, so we consider sv.gersteinlab.org not secure.
Load time
0.266 seconds
SSL
NOT SECURE
Internet Address
128.36.196.120

SERVER OPERATING SYSTEM AND ENCODING

I revealed that sv.gersteinlab.org is operating the Apache/2.2.3 (CentOS) os.

TITLE

Gerstein Lab Structural Variations

DESCRIPTION

Portal for genome SV research in the Gerstein Lab. Personal genome constructor, it can be used to construct a personal diploid genome sequence by including personal variants into reference genome. A tool for CNV discovery and genotyping from depth of read mapping. A tools that implements an algorithm for optimal alignment of sequences with SVs. A pipeline for annotation, classification and analysis of SVs at single nucleotide resolution. Nat Biotechnol. 2010 Jan;28147-55. Epub 2009 Dec 27. Science46.

CONTENT

This web site states the following, "Portal for genome SV research in the Gerstein Lab." Our analyzers noticed that the web site stated " Personal genome constructor, it can be used to construct a personal diploid genome sequence by including personal variants into reference genome." The Website also said " A tool for CNV discovery and genotyping from depth of read mapping. A tools that implements an algorithm for optimal alignment of sequences with SVs. A pipeline for annotation, classification and analysis of SVs at single nucleotide resolution."

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