NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , |
|---|---|
| Format: | Tagungsbericht |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | S200 |
|---|---|
| container_issue | |
| container_start_page | S200 |
| container_title | |
| container_volume | 49 |
| creator | Lespagnol, A. Ndiaye, B. Mosser, Annick Chaplais, C. Gourdet, H. Guenot, Frédérique Bouvet, Régis Moron, G. Mosser, J. de Tayrac, M. |
| description | |
| format | Conference Proceeding |
| fullrecord | <record><control><sourceid>hal</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00935121v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_HAL_hal_00935121v1</sourcerecordid><originalsourceid>FETCH-hal_primary_oai_HAL_hal_00935121v13</originalsourceid><addsrcrecordid>eNqVjMFOwzAQRHMAiUL5h71yCLJpIxpuFWroAaFKIK7R1tk0RrHXeO1K_R5-FCL1BzjNaN7MXBQzVVd1uVLL-qq4FvlSSj2ulmpW_Ly9vENATyN86nsNPUdIA0HknKwn6IgCCH1n8sb6Q7lHoQ46iwfPkqwB7kHY4WQHThI4TfuIZ-xy-mPsBdhD0-w2kLLjHOUJ1hAiSyCT7JFAUu5O01ulFBj0hiIIujCSzIvLHkeh27PeFHfN5uN5Ww44tiFah_HUMtp2u35tp0ypelHpB33Ui_90fwHwNF_O</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>conference_proceeding</recordtype></control><display><type>conference_proceeding</type><title>NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples</title><source>Elsevier ScienceDirect Journals</source><creator>Lespagnol, A. ; Ndiaye, B. ; Mosser, Annick ; Chaplais, C. ; Gourdet, H. ; Guenot, Frédérique ; Bouvet, Régis ; Moron, G. ; Mosser, J. ; de Tayrac, M.</creator><creatorcontrib>Lespagnol, A. ; Ndiaye, B. ; Mosser, Annick ; Chaplais, C. ; Gourdet, H. ; Guenot, Frédérique ; Bouvet, Régis ; Moron, G. ; Mosser, J. ; de Tayrac, M.</creatorcontrib><identifier>ISSN: 0959-8049</identifier><language>eng</language><publisher>Elsevier</publisher><subject>Cancer ; Life Sciences</subject><ispartof>European journal of cancer (1990), 2013, Vol.49, p.S200-S200</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-8165-9525 ; 0000-0001-8165-9525</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,309,310,776,780,785,786,881,23910,23911,25119</link.rule.ids><backlink>$$Uhttps://univ-rennes.hal.science/hal-00935121$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Lespagnol, A.</creatorcontrib><creatorcontrib>Ndiaye, B.</creatorcontrib><creatorcontrib>Mosser, Annick</creatorcontrib><creatorcontrib>Chaplais, C.</creatorcontrib><creatorcontrib>Gourdet, H.</creatorcontrib><creatorcontrib>Guenot, Frédérique</creatorcontrib><creatorcontrib>Bouvet, Régis</creatorcontrib><creatorcontrib>Moron, G.</creatorcontrib><creatorcontrib>Mosser, J.</creatorcontrib><creatorcontrib>de Tayrac, M.</creatorcontrib><title>NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples</title><title>European journal of cancer (1990)</title><subject>Cancer</subject><subject>Life Sciences</subject><issn>0959-8049</issn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2013</creationdate><recordtype>conference_proceeding</recordtype><recordid>eNqVjMFOwzAQRHMAiUL5h71yCLJpIxpuFWroAaFKIK7R1tk0RrHXeO1K_R5-FCL1BzjNaN7MXBQzVVd1uVLL-qq4FvlSSj2ulmpW_Ly9vENATyN86nsNPUdIA0HknKwn6IgCCH1n8sb6Q7lHoQ46iwfPkqwB7kHY4WQHThI4TfuIZ-xy-mPsBdhD0-w2kLLjHOUJ1hAiSyCT7JFAUu5O01ulFBj0hiIIujCSzIvLHkeh27PeFHfN5uN5Ww44tiFah_HUMtp2u35tp0ypelHpB33Ui_90fwHwNF_O</recordid><startdate>201309</startdate><enddate>201309</enddate><creator>Lespagnol, A.</creator><creator>Ndiaye, B.</creator><creator>Mosser, Annick</creator><creator>Chaplais, C.</creator><creator>Gourdet, H.</creator><creator>Guenot, Frédérique</creator><creator>Bouvet, Régis</creator><creator>Moron, G.</creator><creator>Mosser, J.</creator><creator>de Tayrac, M.</creator><general>Elsevier</general><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-8165-9525</orcidid><orcidid>https://orcid.org/0000-0001-8165-9525</orcidid></search><sort><creationdate>201309</creationdate><title>NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples</title><author>Lespagnol, A. ; Ndiaye, B. ; Mosser, Annick ; Chaplais, C. ; Gourdet, H. ; Guenot, Frédérique ; Bouvet, Régis ; Moron, G. ; Mosser, J. ; de Tayrac, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-hal_primary_oai_HAL_hal_00935121v13</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Cancer</topic><topic>Life Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lespagnol, A.</creatorcontrib><creatorcontrib>Ndiaye, B.</creatorcontrib><creatorcontrib>Mosser, Annick</creatorcontrib><creatorcontrib>Chaplais, C.</creatorcontrib><creatorcontrib>Gourdet, H.</creatorcontrib><creatorcontrib>Guenot, Frédérique</creatorcontrib><creatorcontrib>Bouvet, Régis</creatorcontrib><creatorcontrib>Moron, G.</creatorcontrib><creatorcontrib>Mosser, J.</creatorcontrib><creatorcontrib>de Tayrac, M.</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lespagnol, A.</au><au>Ndiaye, B.</au><au>Mosser, Annick</au><au>Chaplais, C.</au><au>Gourdet, H.</au><au>Guenot, Frédérique</au><au>Bouvet, Régis</au><au>Moron, G.</au><au>Mosser, J.</au><au>de Tayrac, M.</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples</atitle><btitle>European journal of cancer (1990)</btitle><date>2013-09</date><risdate>2013</risdate><volume>49</volume><spage>S200</spage><epage>S200</epage><pages>S200-S200</pages><issn>0959-8049</issn><pub>Elsevier</pub><orcidid>https://orcid.org/0000-0001-8165-9525</orcidid><orcidid>https://orcid.org/0000-0001-8165-9525</orcidid></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0959-8049 |
| ispartof | European journal of cancer (1990), 2013, Vol.49, p.S200-S200 |
| issn | 0959-8049 |
| language | eng |
| recordid | cdi_hal_primary_oai_HAL_hal_00935121v1 |
| source | Elsevier ScienceDirect Journals |
| subjects | Cancer Life Sciences |
| title | NGS panel V1.1 for the routine deep sequencing-based diagnostic of somatic hotspot theranostic mutations on FFPE tumours: A prospective study of 500 cancer samples |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T09%3A22%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-hal&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=proceeding&rft.atitle=NGS%20panel%20V1.1%20for%20the%20routine%20deep%20sequencing-based%20diagnostic%20of%20somatic%20hotspot%20theranostic%20mutations%20on%20FFPE%20tumours:%20A%20prospective%20study%20of%20500%20cancer%20samples&rft.btitle=European%20journal%20of%20cancer%20(1990)&rft.au=Lespagnol,%20A.&rft.date=2013-09&rft.volume=49&rft.spage=S200&rft.epage=S200&rft.pages=S200-S200&rft.issn=0959-8049&rft_id=info:doi/&rft_dat=%3Chal%3Eoai_HAL_hal_00935121v1%3C/hal%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |