215016bf4adff3d8b957c388af767583214db924 abenetpa Wed Sep 30 07:29:04 2020 -0700 added filters and CNV color to description refs#25841 diff --git src/hg/makeDb/trackDb/human/decipher.html src/hg/makeDb/trackDb/human/decipher.html index 4c9d4f8..3b1c9c4 100644 --- src/hg/makeDb/trackDb/human/decipher.html +++ src/hg/makeDb/trackDb/human/decipher.html @@ -40,51 +40,72 @@ <P> The <A HREF="https://decipher.sanger.ac.uk" TARGET=_BLANK>DECIPHER</A> database of submicroscopic chromosomal imbalance collects clinical information about chromosomal microdeletions/duplications/insertions, translocations and inversions, and displays this information on the human genome map. <p> This track shows genomic regions of reported cases and their associated phenotype information. All data have passed the strict consent requirements of the DECIPHER project and are approved for unrestricted public release. Clicking the Patient View ID link brings up a more detailed informational page on the patient at the DECIPHER web site. -<H2>Method</H2> + +<H2>Display Conventions and Configuration</H2> <P> -Data provided by the DECIPHER project group are imported and processed -to create a simple BED track to annotate the genomic regions associated -with individual patients. -</P> +The genomic locations of DECIPHER variants are labelled with the DECIPHER variant descriptions. +<b>Mouseover</b> on items shows variant details, clinical interpretation, and associated conditions. +Further information on each variant is displayed on the details page by a click onto any variant. +</p> + +<P> +For the <b>CNVs track</b>, the entries are colored by the <b>type of variant</b>: <ul> - <li> - For the CNVs track, the entries are colored <B><FONT COLOR = RED>red</FONT></B> for deletions - (mean log ratio < 0) and <B><FONT COLOR = BLUE>blue</FONT></B> for duplications - (mean log ratio > 0). Entries where no mean ratio is available are colored - <b><font color="#888">grey</font></b>.</li> - <li> - For the SNVs track, the entries are colored according to the estimated pathogenicity of the - variant. <br>Entries are colored: + <li><b><font color="red">red</font></b> for loss</li> + <li><b><font color="blue">blue</font></b> for gain</li> + <li><b><font color="grey">grey</font></b> for amplification</li> +</ul> +</P> + +<P> +A light-to-dark color gradient indicates the <b>clinical significance</b> of each variant, with +the lightest shade being benign, to the darkest shade being pathogenic. Detailed information on the +CNV color code is described <a href="https://genome.ucsc.edu/goldenPath/help/hgCnvColoring.html">here</a>. +Items can be filtered according to the size of the variant, variant type, and clinical significance +using the track <b>Configure</b> options. +</P> + +<P> +For the <b>SNVs track</b>, the entries are colored according to the estimated <b>clinical significance</b> +of the variant: <ul> <li><b><font color="black">black</font></b> for likely or definitely pathogenic</li> <li><b><font color="#888">dark grey</font></b> for uncertain or unknown</li> <li><b><font color="#c8c8c8">light grey</font></b> for likely or definitely benign</li> </ul> -</ul> +</P> + +<H2>Method</H2> +<P> +Data provided by the DECIPHER project group are imported and processed +to create a simple BED track to annotate the genomic regions associated +with individual patients. +</P> + <H2>Contact</H2> <P> For more information on DECIPHER, please contact <A HREF="mailto:decipher@sanger. ac. uk"> decipher@sanger.ac.uk</A>. </P> <H2>References</H2> <p> Firth HV, Richards SM, Bevan AP, Clayton S, Corpas M, Rajan D, Van Vooren S, Moreau Y, Pettett RM, Carter NP. <a href="https://www.cell.com/ajhg/abstract/S0002-9297(09)00107-4" target="_blank">