Loading…
Feasibility of Optical Genome Mapping in Cytogenetic Diagnostics of Hematological Neoplasms: A New Way to Look at DNA
Optical genome mapping (OGM) is a new genome-wide technology that can reveal both structural genomic variations (SVs) and copy number variations (CNVs) in a single assay. OGM was initially employed to perform genome assembly and genome research, but it is now more widely used to study chromosome abe...
Saved in:
Published in: | Diagnostics (Basel) 2023-05, Vol.13 (11), p.1841 |
---|---|
Main Authors: | , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c567t-4c21baac141bf62d68e7c979fbd95b49b9391b6eb932b64acf3921586c08872e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c567t-4c21baac141bf62d68e7c979fbd95b49b9391b6eb932b64acf3921586c08872e3 |
container_end_page | |
container_issue | 11 |
container_start_page | 1841 |
container_title | Diagnostics (Basel) |
container_volume | 13 |
creator | Coccaro, Nicoletta Anelli, Luisa Zagaria, Antonella Tarantini, Francesco Cumbo, Cosimo Tota, Giuseppina Minervini, Crescenzio Francesco Minervini, Angela Conserva, Maria Rosa Redavid, Immacolata Parciante, Elisa Macchia, Maria Giovanna Specchia, Giorgina Musto, Pellegrino Albano, Francesco |
description | Optical genome mapping (OGM) is a new genome-wide technology that can reveal both structural genomic variations (SVs) and copy number variations (CNVs) in a single assay. OGM was initially employed to perform genome assembly and genome research, but it is now more widely used to study chromosome aberrations in genetic disorders and in human cancer. One of the most useful OGM applications is in hematological malignancies, where chromosomal rearrangements are frequent and conventional cytogenetic analysis alone is insufficient, necessitating further confirmation using ancillary techniques such as fluorescence in situ hybridization, chromosomal microarrays, or multiple ligation-dependent probe amplification. The first studies tested OGM efficiency and sensitivity for SV and CNV detection, comparing heterogeneous groups of lymphoid and myeloid hematological sample data with those obtained using standard cytogenetic diagnostic tests. Most of the work based on this innovative technology was focused on myelodysplastic syndromes (MDSs), acute myeloid leukemia (AML), and acute lymphoblastic leukemia (ALL), whereas little attention was paid to chronic lymphocytic leukemia (CLL) or multiple myeloma (MM), and none was paid to lymphomas. The studies showed that OGM can now be considered as a highly reliable method, concordant with standard cytogenetic techniques but able to detect novel clinically significant SVs, thus allowing better patient classification, prognostic stratification, and therapeutic choices in hematological malignancies. |
doi_str_mv | 10.3390/diagnostics13111841 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_50243c36f6fe4f5a829cf10b26071654</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A752474466</galeid><doaj_id>oai_doaj_org_article_50243c36f6fe4f5a829cf10b26071654</doaj_id><sourcerecordid>A752474466</sourcerecordid><originalsourceid>FETCH-LOGICAL-c567t-4c21baac141bf62d68e7c979fbd95b49b9391b6eb932b64acf3921586c08872e3</originalsourceid><addsrcrecordid>eNptUk1v1DAQjRCIVqW_AAlZ4sJl2_gjjs0Frbb0Q1raC4ijZTvj4CWxQ5wt2n9fb7e0XVT7MPbMe2_0RlMU73F5QqksTxuv2xDT5G3CFGMsGH5VHJKyrmaMYfH62fugOE5pVeYjMRWkelsc0JpIziU9LNbnoJM3vvPTBkWHboYsqTt0ASH2gL7pYfChRT6gxWaKLQTIdXT21H1LuoReT7GL7T31GuLQ6dSnz2ieP3_RT71BU0TLGH8jPaGz6_m74o3TXYLjh3hU_Dj_-n1xOVveXFwt5suZrXg9zZgl2GhtMcPGcdJwAbWVtXSmkZVh0kgqseGQIzGcaeuoJLgS3JZC1AToUXG1022iXqlh9L0eNypqr-4TcWyVHrOLDlRVEkYt5Y47YK7SgkjrcGkIL2vMK5a1vuy0hrXpobEQplF3e6L7leB_qTbeKlySilBMssKnB4Ux_llDmlTvk4Wu0wHiOikiCOOizh4y9ON_0FVcjyHPaouieQYciydUq7MDH1zMje1WVM3rirCaMc4z6uQFVL4N9N7GAM7n_B6B7gh2jCmN4B5N4lJtt0-9sH2Z9eH5fB45_3aN3gG68tZa</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2823979618</pqid></control><display><type>article</type><title>Feasibility of Optical Genome Mapping in Cytogenetic Diagnostics of Hematological Neoplasms: A New Way to Look at DNA</title><source>PubMed (Medline)</source><source>Publicly Available Content Database</source><creator>Coccaro, Nicoletta ; Anelli, Luisa ; Zagaria, Antonella ; Tarantini, Francesco ; Cumbo, Cosimo ; Tota, Giuseppina ; Minervini, Crescenzio Francesco ; Minervini, Angela ; Conserva, Maria Rosa ; Redavid, Immacolata ; Parciante, Elisa ; Macchia, Maria Giovanna ; Specchia, Giorgina ; Musto, Pellegrino ; Albano, Francesco</creator><creatorcontrib>Coccaro, Nicoletta ; Anelli, Luisa ; Zagaria, Antonella ; Tarantini, Francesco ; Cumbo, Cosimo ; Tota, Giuseppina ; Minervini, Crescenzio Francesco ; Minervini, Angela ; Conserva, Maria Rosa ; Redavid, Immacolata ; Parciante, Elisa ; Macchia, Maria Giovanna ; Specchia, Giorgina ; Musto, Pellegrino ; Albano, Francesco</creatorcontrib><description>Optical genome mapping (OGM) is a new genome-wide technology that can reveal both structural genomic variations (SVs) and copy number variations (CNVs) in a single assay. OGM was initially employed to perform genome assembly and genome research, but it is now more widely used to study chromosome aberrations in genetic disorders and in human cancer. One of the most useful OGM applications is in hematological malignancies, where chromosomal rearrangements are frequent and conventional cytogenetic analysis alone is insufficient, necessitating further confirmation using ancillary techniques such as fluorescence in situ hybridization, chromosomal microarrays, or multiple ligation-dependent probe amplification. The first studies tested OGM efficiency and sensitivity for SV and CNV detection, comparing heterogeneous groups of lymphoid and myeloid hematological sample data with those obtained using standard cytogenetic diagnostic tests. Most of the work based on this innovative technology was focused on myelodysplastic syndromes (MDSs), acute myeloid leukemia (AML), and acute lymphoblastic leukemia (ALL), whereas little attention was paid to chronic lymphocytic leukemia (CLL) or multiple myeloma (MM), and none was paid to lymphomas. The studies showed that OGM can now be considered as a highly reliable method, concordant with standard cytogenetic techniques but able to detect novel clinically significant SVs, thus allowing better patient classification, prognostic stratification, and therapeutic choices in hematological malignancies.</description><identifier>ISSN: 2075-4418</identifier><identifier>EISSN: 2075-4418</identifier><identifier>DOI: 10.3390/diagnostics13111841</identifier><identifier>PMID: 37296693</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Analysis ; Cancer ; Chromosomes ; Cytogenetics ; DNA ; Enzymes ; Genes ; Genetic aspects ; Genomes ; Genomics ; hematologic neoplasms ; Hematology ; Labeling ; Laboratories ; Leukemia ; Lymphomas ; Methods ; Oncology, Experimental ; optical genome mapping ; Review</subject><ispartof>Diagnostics (Basel), 2023-05, Vol.13 (11), p.1841</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c567t-4c21baac141bf62d68e7c979fbd95b49b9391b6eb932b64acf3921586c08872e3</citedby><cites>FETCH-LOGICAL-c567t-4c21baac141bf62d68e7c979fbd95b49b9391b6eb932b64acf3921586c08872e3</cites><orcidid>0000-0003-3277-6594 ; 0000-0002-3323-6445 ; 0000-0002-9185-724X ; 0000-0001-7926-6052 ; 0000-0002-2509-6200 ; 0000-0002-4382-9906</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2823979618/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2823979618?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37296693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Coccaro, Nicoletta</creatorcontrib><creatorcontrib>Anelli, Luisa</creatorcontrib><creatorcontrib>Zagaria, Antonella</creatorcontrib><creatorcontrib>Tarantini, Francesco</creatorcontrib><creatorcontrib>Cumbo, Cosimo</creatorcontrib><creatorcontrib>Tota, Giuseppina</creatorcontrib><creatorcontrib>Minervini, Crescenzio Francesco</creatorcontrib><creatorcontrib>Minervini, Angela</creatorcontrib><creatorcontrib>Conserva, Maria Rosa</creatorcontrib><creatorcontrib>Redavid, Immacolata</creatorcontrib><creatorcontrib>Parciante, Elisa</creatorcontrib><creatorcontrib>Macchia, Maria Giovanna</creatorcontrib><creatorcontrib>Specchia, Giorgina</creatorcontrib><creatorcontrib>Musto, Pellegrino</creatorcontrib><creatorcontrib>Albano, Francesco</creatorcontrib><title>Feasibility of Optical Genome Mapping in Cytogenetic Diagnostics of Hematological Neoplasms: A New Way to Look at DNA</title><title>Diagnostics (Basel)</title><addtitle>Diagnostics (Basel)</addtitle><description>Optical genome mapping (OGM) is a new genome-wide technology that can reveal both structural genomic variations (SVs) and copy number variations (CNVs) in a single assay. OGM was initially employed to perform genome assembly and genome research, but it is now more widely used to study chromosome aberrations in genetic disorders and in human cancer. One of the most useful OGM applications is in hematological malignancies, where chromosomal rearrangements are frequent and conventional cytogenetic analysis alone is insufficient, necessitating further confirmation using ancillary techniques such as fluorescence in situ hybridization, chromosomal microarrays, or multiple ligation-dependent probe amplification. The first studies tested OGM efficiency and sensitivity for SV and CNV detection, comparing heterogeneous groups of lymphoid and myeloid hematological sample data with those obtained using standard cytogenetic diagnostic tests. Most of the work based on this innovative technology was focused on myelodysplastic syndromes (MDSs), acute myeloid leukemia (AML), and acute lymphoblastic leukemia (ALL), whereas little attention was paid to chronic lymphocytic leukemia (CLL) or multiple myeloma (MM), and none was paid to lymphomas. The studies showed that OGM can now be considered as a highly reliable method, concordant with standard cytogenetic techniques but able to detect novel clinically significant SVs, thus allowing better patient classification, prognostic stratification, and therapeutic choices in hematological malignancies.</description><subject>Analysis</subject><subject>Cancer</subject><subject>Chromosomes</subject><subject>Cytogenetics</subject><subject>DNA</subject><subject>Enzymes</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Genomics</subject><subject>hematologic neoplasms</subject><subject>Hematology</subject><subject>Labeling</subject><subject>Laboratories</subject><subject>Leukemia</subject><subject>Lymphomas</subject><subject>Methods</subject><subject>Oncology, Experimental</subject><subject>optical genome mapping</subject><subject>Review</subject><issn>2075-4418</issn><issn>2075-4418</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIVqW_AAlZ4sJl2_gjjs0Frbb0Q1raC4ijZTvj4CWxQ5wt2n9fb7e0XVT7MPbMe2_0RlMU73F5QqksTxuv2xDT5G3CFGMsGH5VHJKyrmaMYfH62fugOE5pVeYjMRWkelsc0JpIziU9LNbnoJM3vvPTBkWHboYsqTt0ASH2gL7pYfChRT6gxWaKLQTIdXT21H1LuoReT7GL7T31GuLQ6dSnz2ieP3_RT71BU0TLGH8jPaGz6_m74o3TXYLjh3hU_Dj_-n1xOVveXFwt5suZrXg9zZgl2GhtMcPGcdJwAbWVtXSmkZVh0kgqseGQIzGcaeuoJLgS3JZC1AToUXG1022iXqlh9L0eNypqr-4TcWyVHrOLDlRVEkYt5Y47YK7SgkjrcGkIL2vMK5a1vuy0hrXpobEQplF3e6L7leB_qTbeKlySilBMssKnB4Ux_llDmlTvk4Wu0wHiOikiCOOizh4y9ON_0FVcjyHPaouieQYciydUq7MDH1zMje1WVM3rirCaMc4z6uQFVL4N9N7GAM7n_B6B7gh2jCmN4B5N4lJtt0-9sH2Z9eH5fB45_3aN3gG68tZa</recordid><startdate>20230524</startdate><enddate>20230524</enddate><creator>Coccaro, Nicoletta</creator><creator>Anelli, Luisa</creator><creator>Zagaria, Antonella</creator><creator>Tarantini, Francesco</creator><creator>Cumbo, Cosimo</creator><creator>Tota, Giuseppina</creator><creator>Minervini, Crescenzio Francesco</creator><creator>Minervini, Angela</creator><creator>Conserva, Maria Rosa</creator><creator>Redavid, Immacolata</creator><creator>Parciante, Elisa</creator><creator>Macchia, Maria Giovanna</creator><creator>Specchia, Giorgina</creator><creator>Musto, Pellegrino</creator><creator>Albano, Francesco</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3277-6594</orcidid><orcidid>https://orcid.org/0000-0002-3323-6445</orcidid><orcidid>https://orcid.org/0000-0002-9185-724X</orcidid><orcidid>https://orcid.org/0000-0001-7926-6052</orcidid><orcidid>https://orcid.org/0000-0002-2509-6200</orcidid><orcidid>https://orcid.org/0000-0002-4382-9906</orcidid></search><sort><creationdate>20230524</creationdate><title>Feasibility of Optical Genome Mapping in Cytogenetic Diagnostics of Hematological Neoplasms: A New Way to Look at DNA</title><author>Coccaro, Nicoletta ; Anelli, Luisa ; Zagaria, Antonella ; Tarantini, Francesco ; Cumbo, Cosimo ; Tota, Giuseppina ; Minervini, Crescenzio Francesco ; Minervini, Angela ; Conserva, Maria Rosa ; Redavid, Immacolata ; Parciante, Elisa ; Macchia, Maria Giovanna ; Specchia, Giorgina ; Musto, Pellegrino ; Albano, Francesco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c567t-4c21baac141bf62d68e7c979fbd95b49b9391b6eb932b64acf3921586c08872e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Analysis</topic><topic>Cancer</topic><topic>Chromosomes</topic><topic>Cytogenetics</topic><topic>DNA</topic><topic>Enzymes</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genomes</topic><topic>Genomics</topic><topic>hematologic neoplasms</topic><topic>Hematology</topic><topic>Labeling</topic><topic>Laboratories</topic><topic>Leukemia</topic><topic>Lymphomas</topic><topic>Methods</topic><topic>Oncology, Experimental</topic><topic>optical genome mapping</topic><topic>Review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Coccaro, Nicoletta</creatorcontrib><creatorcontrib>Anelli, Luisa</creatorcontrib><creatorcontrib>Zagaria, Antonella</creatorcontrib><creatorcontrib>Tarantini, Francesco</creatorcontrib><creatorcontrib>Cumbo, Cosimo</creatorcontrib><creatorcontrib>Tota, Giuseppina</creatorcontrib><creatorcontrib>Minervini, Crescenzio Francesco</creatorcontrib><creatorcontrib>Minervini, Angela</creatorcontrib><creatorcontrib>Conserva, Maria Rosa</creatorcontrib><creatorcontrib>Redavid, Immacolata</creatorcontrib><creatorcontrib>Parciante, Elisa</creatorcontrib><creatorcontrib>Macchia, Maria Giovanna</creatorcontrib><creatorcontrib>Specchia, Giorgina</creatorcontrib><creatorcontrib>Musto, Pellegrino</creatorcontrib><creatorcontrib>Albano, Francesco</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Diagnostics (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coccaro, Nicoletta</au><au>Anelli, Luisa</au><au>Zagaria, Antonella</au><au>Tarantini, Francesco</au><au>Cumbo, Cosimo</au><au>Tota, Giuseppina</au><au>Minervini, Crescenzio Francesco</au><au>Minervini, Angela</au><au>Conserva, Maria Rosa</au><au>Redavid, Immacolata</au><au>Parciante, Elisa</au><au>Macchia, Maria Giovanna</au><au>Specchia, Giorgina</au><au>Musto, Pellegrino</au><au>Albano, Francesco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Feasibility of Optical Genome Mapping in Cytogenetic Diagnostics of Hematological Neoplasms: A New Way to Look at DNA</atitle><jtitle>Diagnostics (Basel)</jtitle><addtitle>Diagnostics (Basel)</addtitle><date>2023-05-24</date><risdate>2023</risdate><volume>13</volume><issue>11</issue><spage>1841</spage><pages>1841-</pages><issn>2075-4418</issn><eissn>2075-4418</eissn><abstract>Optical genome mapping (OGM) is a new genome-wide technology that can reveal both structural genomic variations (SVs) and copy number variations (CNVs) in a single assay. OGM was initially employed to perform genome assembly and genome research, but it is now more widely used to study chromosome aberrations in genetic disorders and in human cancer. One of the most useful OGM applications is in hematological malignancies, where chromosomal rearrangements are frequent and conventional cytogenetic analysis alone is insufficient, necessitating further confirmation using ancillary techniques such as fluorescence in situ hybridization, chromosomal microarrays, or multiple ligation-dependent probe amplification. The first studies tested OGM efficiency and sensitivity for SV and CNV detection, comparing heterogeneous groups of lymphoid and myeloid hematological sample data with those obtained using standard cytogenetic diagnostic tests. Most of the work based on this innovative technology was focused on myelodysplastic syndromes (MDSs), acute myeloid leukemia (AML), and acute lymphoblastic leukemia (ALL), whereas little attention was paid to chronic lymphocytic leukemia (CLL) or multiple myeloma (MM), and none was paid to lymphomas. The studies showed that OGM can now be considered as a highly reliable method, concordant with standard cytogenetic techniques but able to detect novel clinically significant SVs, thus allowing better patient classification, prognostic stratification, and therapeutic choices in hematological malignancies.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37296693</pmid><doi>10.3390/diagnostics13111841</doi><orcidid>https://orcid.org/0000-0003-3277-6594</orcidid><orcidid>https://orcid.org/0000-0002-3323-6445</orcidid><orcidid>https://orcid.org/0000-0002-9185-724X</orcidid><orcidid>https://orcid.org/0000-0001-7926-6052</orcidid><orcidid>https://orcid.org/0000-0002-2509-6200</orcidid><orcidid>https://orcid.org/0000-0002-4382-9906</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2075-4418 |
ispartof | Diagnostics (Basel), 2023-05, Vol.13 (11), p.1841 |
issn | 2075-4418 2075-4418 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_50243c36f6fe4f5a829cf10b26071654 |
source | PubMed (Medline); Publicly Available Content Database |
subjects | Analysis Cancer Chromosomes Cytogenetics DNA Enzymes Genes Genetic aspects Genomes Genomics hematologic neoplasms Hematology Labeling Laboratories Leukemia Lymphomas Methods Oncology, Experimental optical genome mapping Review |
title | Feasibility of Optical Genome Mapping in Cytogenetic Diagnostics of Hematological Neoplasms: A New Way to Look at DNA |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T21%3A01%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Feasibility%20of%20Optical%20Genome%20Mapping%20in%20Cytogenetic%20Diagnostics%20of%20Hematological%20Neoplasms:%20A%20New%20Way%20to%20Look%20at%20DNA&rft.jtitle=Diagnostics%20(Basel)&rft.au=Coccaro,%20Nicoletta&rft.date=2023-05-24&rft.volume=13&rft.issue=11&rft.spage=1841&rft.pages=1841-&rft.issn=2075-4418&rft.eissn=2075-4418&rft_id=info:doi/10.3390/diagnostics13111841&rft_dat=%3Cgale_doaj_%3EA752474466%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c567t-4c21baac141bf62d68e7c979fbd95b49b9391b6eb932b64acf3921586c08872e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2823979618&rft_id=info:pmid/37296693&rft_galeid=A752474466&rfr_iscdi=true |