blank Quick help
blank Maintenance news

Scheduled maintenance

Regular maintenance outages:
between 05.00 and 05.15 hrs CET (Monday to Sunday).

Other outages
Availability

2022.02.11

More...
blank News flashes

News Flashes

New version of the European Patent Register – SPC proceedings information in the Unitary Patent Register.

2024-07-24

More...
blank Related links

Extract from the Register of European Patents

EP About this file: EP3303624

EP3303624 - METHODS FOR ENHANCED CGH ANALYSIS [Right-click to bookmark this link]
Former [2018/15]METHODS, SUPPORTS AND KITS FOR ENHANCED CGH ANALYSIS
[2020/51]
StatusNo opposition filed within time limit
Status updated on  25.03.2022
Database last updated on 19.10.2024
FormerThe patent has been granted
Status updated on  16.04.2021
FormerGrant of patent is intended
Status updated on  06.12.2020
FormerExamination is in progress
Status updated on  18.10.2019
FormerRequest for examination was made
Status updated on  09.03.2018
FormerThe international publication has been made
Status updated on  09.12.2016
Most recent event   Tooltip13.09.2024Lapse of the patent in a contracting state
New state(s): MT
published on 16.10.2024  [2024/42]
Applicant(s)For all designated states
Altergon S.A.
Via Dogana Vecchia 2
6901 Lugano / CH
[2018/15]
Inventor(s)01 / IANNONE, Mariano
c/o Altergon SA
Via Dogana Vecchia, 2
6901 Lugano / CH
02 / AMOROSI, Stefania
c/o Altergon SA
Via Dogana Vecchia, 2
6901 Lugano / CH
03 / PICCININNI, Sabina
c/o Altergon SA
Via Dogana Vecchia, 2
6901 Lugano / CH
04 / FOSSATI, Tiziano
c/o Altergon SA
Via Dogana Vecchia, 2
6901 Lugano / CH
 [2021/20]
Former [2018/15]01 / IANNONE, Mariano
c/o ALTERGON SA
Via Dogana Vecchia 2
6901 Lugano / CH
02 / AMOROSI, Stefania
c/o ALTERGON SA
Via Dogana Vecchia 2
6901 Lugano / CH
03 / PICCININNI, Sabina
c/o ALTERGON SA
Via Dogana Vecchia 2
6901 Lugano / CH
04 / FOSSATI, Tiziano
c/o ALTERGON SA
Via Dogana Vecchia 2
6901 Lugano / CH
Representative(s)Gerli, Paolo
Botti & Ferrari S.p.A.
Via Cappellini, 11
20124 Milano / IT
[2021/20]
Former [2018/15]Gerli, Paolo
Botti & Ferrari S.r.l. Via Cappellini, 11
20124 Milano / IT
Application number, filing date16729798.525.05.2016
[2018/15]
WO2016EP61764
Priority number, dateEP2015016994729.05.2015         Original published format: EP 15169947
[2018/15]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2016193084
Date:08.12.2016
Language:EN
[2016/49]
Type: A1 Application with search report 
No.:EP3303624
Date:11.04.2018
Language:EN
The application published by WIPO in one of the EPO official languages on 08.12.2016 takes the place of the publication of the European patent application.
[2018/15]
Type: B1 Patent specification 
No.:EP3303624
Date:19.05.2021
Language:EN
[2021/20]
Search report(s)International search report - published on:EP08.12.2016
ClassificationIPC:C12Q1/6827
[2020/50]
CPC:
C12Q1/6827 (EP,CN,KR,US); C12Q1/6809 (EP,CN,KR,US); C12Q1/68 (RU);
C12Q2537/16 (KR); C12Q2545/113 (KR); C12Q2600/156 (EP,US)
Former IPC [2018/15]C12Q1/68
Designated contracting statesAL,   AT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   MK,   MT,   NL,   NO,   PL,   PT,   RO,   RS,   SE,   SI,   SK,   SM,   TR [2018/15]
Extension statesBANot yet paid
MENot yet paid
Validation statesMANot yet paid
MDNot yet paid
TitleGerman:VERFAHREN ZUR VERBESSERTEN CGH-ANALYSE[2020/51]
English:METHODS FOR ENHANCED CGH ANALYSIS[2020/51]
French:PROCÉDÉS POUR L'ANALYSE AMÉLIORÉE D'UN SIMULATEUR CGH[2020/51]
Former [2018/15]VERFAHREN, TRÄGER UND KITS ZUR VERBESSERTEN CGH-ANALYSE
Former [2018/15]METHODS, SUPPORTS AND KITS FOR ENHANCED CGH ANALYSIS
Former [2018/15]PROCÉDÉS, SUPPORTS ET NÉCESSAIRES PERMETTANT UNE MEILLEURE ANALYSE CGH
Entry into regional phase20.12.2017National basic fee paid 
20.12.2017Designation fee(s) paid 
20.12.2017Examination fee paid 
Examination procedure20.12.2017Examination requested  [2018/15]
20.12.2017Date on which the examining division has become responsible
18.06.2018Amendment by applicant (claims and/or description)
22.10.2019Despatch of a communication from the examining division (Time limit: M06)
17.04.2020Reply to a communication from the examining division
07.12.2020Communication of intention to grant the patent
06.04.2021Fee for grant paid
06.04.2021Fee for publishing/printing paid
06.04.2021Receipt of the translation of the claim(s)
Opposition(s)22.02.2022No opposition filed within time limit [2022/17]
Fees paidRenewal fee
25.05.2018Renewal fee patent year 03
21.05.2019Renewal fee patent year 04
20.05.2020Renewal fee patent year 05
Opt-out from the exclusive  Tooltip
competence of the Unified
Patent Court
See the Register of the Unified Patent Court for opt-out data
Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Lapses during opposition  TooltipHU25.05.2016
AL19.05.2021
AT19.05.2021
CY19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
MK19.05.2021
MT19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SI19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
BE31.05.2021
FR19.07.2021
BG19.08.2021
GB19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
[2024/42]
Former [2024/22]HU25.05.2016
AL19.05.2021
AT19.05.2021
CY19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
MK19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SI19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
BE31.05.2021
FR19.07.2021
BG19.08.2021
GB19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2023/30]HU25.05.2016
AL19.05.2021
AT19.05.2021
CY19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SI19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
BE31.05.2021
FR19.07.2021
BG19.08.2021
GB19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2023/29]HU25.05.2016
AL19.05.2021
AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SI19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
BE31.05.2021
FR19.07.2021
BG19.08.2021
GB19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2022/35]AL19.05.2021
AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SI19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
BE31.05.2021
FR19.07.2021
BG19.08.2021
GB19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2022/34]AL19.05.2021
AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SI19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
BE31.05.2021
FR19.07.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2022/29]AL19.05.2021
AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SI19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
FR19.07.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2022/26]AL19.05.2021
AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
FR19.07.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2022/23]AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
FR19.07.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
DE01.12.2021
Former [2022/21]AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SK19.05.2021
SM19.05.2021
IE25.05.2021
LU25.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
PT20.09.2021
DE01.12.2021
IS22.12.2021
Former [2022/18]AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
MC19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SK19.05.2021
SM19.05.2021
LU25.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
PT20.09.2021
IS22.12.2021
Former [2022/10]AT19.05.2021
CZ19.05.2021
DK19.05.2021
EE19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SK19.05.2021
SM19.05.2021
LU25.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
PT20.09.2021
IS22.12.2021
Former [2022/09]AT19.05.2021
CZ19.05.2021
DK19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
NL19.05.2021
PL19.05.2021
RO19.05.2021
RS19.05.2021
SE19.05.2021
SK19.05.2021
SM19.05.2021
LU25.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
Former [2022/08]AT19.05.2021
CZ19.05.2021
DK19.05.2021
ES19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
NL19.05.2021
PL19.05.2021
RS19.05.2021
SE19.05.2021
SM19.05.2021
LU25.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
Former [2022/07]AT19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
NL19.05.2021
PL19.05.2021
RS19.05.2021
SE19.05.2021
SM19.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
Former [2022/04]AT19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
NL19.05.2021
PL19.05.2021
RS19.05.2021
SE19.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
Former [2021/52]AT19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
PL19.05.2021
RS19.05.2021
SE19.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
Former [2021/51]AT19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
RS19.05.2021
SE19.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
IS19.09.2021
PT20.09.2021
Former [2021/50]AT19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
SE19.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
PT20.09.2021
Former [2021/49]AT19.05.2021
FI19.05.2021
HR19.05.2021
LT19.05.2021
LV19.05.2021
SE19.05.2021
BG19.08.2021
NO19.08.2021
GR20.08.2021
Former [2021/47]AT19.05.2021
FI19.05.2021
LT19.05.2021
BG19.08.2021
Former [2021/46]AT19.05.2021
FI19.05.2021
LT19.05.2021
Cited inInternational search[A]WO2009062166  (UNIV WASHINGTON [US], et al) [A] 1-17 * abstract * * claims 1,11,23,34,42 *;
 [A]US2008026390  (STOUGHTON ROLAND [US], et al) [A] 1-17 * abstract * * claims 1-2 *;
 [XDI]  - SVETLANA A. YATSENKO ET AL, "Microarray-Based Comparative Genomic Hybridization Using Sex-Matched Reference DNA Provides Greater Sensitivity for Detection of Sex Chromosome Imbalances than Array-Comparative Genomic Hybridization with Sex-Mismatched Reference DNA", JOURNAL OF MOLECULAR DIAGNOSTICS,THE, US, (20090501), vol. 11, no. 3, doi:10.2353/jmoldx.2009.080064, ISSN 1525-1578, pages 226 - 237, XP055233498 [XD] 1-3,5-8,10-12,16,17 * abstract * * page 227 - page 228 * * figures 1-4 * * discussion * [I] 4,9,13-15

DOI:   http://dx.doi.org/10.2353/jmoldx.2009.080064
 [A]  - W. R. LAI ET AL, "Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data", BIOINFORMATICS., GB, (20051001), vol. 21, no. 19, doi:10.1093/bioinformatics/bti611, ISSN 1367-4803, pages 3763 - 3770, XP055233480 [A] 1-17 * abstract * * discussion *

DOI:   http://dx.doi.org/10.1093/bioinformatics/bti611
 [AD]  - A. E. DELLINGER ET AL, "Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays", NUCLEIC ACIDS RESEARCH, GB, (20100501), vol. 38, no. 9, doi:10.1093/nar/gkq040, ISSN 0305-1048, pages e105 - e105, XP055233486 [AD] 1-17 * abstract *

DOI:   http://dx.doi.org/10.1093/nar/gkq040
 [AD]  - PINTO D ET AL, "Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants", NATURE BIOTECHNOLOGY, NATURE PUBLISHING GROUP, UNITED STATES, vol. 29, no. 6, doi:10.1038/NBT.1852, ISSN 1546-1696, (20110601), pages 512 - 520, (20110508), XP002735142 [AD] 1-17 * abstract *

DOI:   http://dx.doi.org/10.1038/nbt.1852
Examination   - H. TÖNNIES ET AL, "First Systematic CGH-based Analyses of Ancient DNA Samples of Malformed Fetuses Preserved in the Meckel Anatomical Collection in Halle/Saale (Germany)", JOURNAL OF HISTOCHEMISTRY AND CYTOCHEMISTRY, US, (20050326), vol. 53, no. 3, doi:10.1369/jhc.4B6427.2005, ISSN 0022-1554, pages 381 - 384, XP055633200

DOI:   http://dx.doi.org/10.1369/jhc.4B6427.2005
by applicantWO2013171565
    - JOO WOOK AHN ET AL., "Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patients", MOLECULAR CYTOGENETICS, (2013), vol. 6, doi:doi:10.1186/1755-8166-6-16, page 16, XP021145831

DOI:   http://dx.doi.org/10.1186/1755-8166-6-16
    - HASSOLD T ET AL., "The origin of human aneuploidy: where we have been, where we are going", HUMAN MOL GENETICS, (200708), vol. 16, no. 2, pages R203 - R20
    - FRAGOULI E ET AL., "Aneuploidy screening for embryo selection", SEMIN REPROD MED., (201208), vol. 30, no. 4, pages 289 - 301
    - YIMER, N.; ROSNINA, "Chromosomal Anomalies and Infertility in Farm Animals: A ReviewY", PERTANIKA J. TROP. AGRIC. SCI., (2014), vol. 37, no. 1, pages 1 - 18
    - BLAZAK, W. F.; ELDRIDGE, F.E., "A Robertsonian translocation and its effect upon fertility in Brown Swiss cattle", JOURNAL OF DAIRY SCIENCE, (1977), vol. 60, no. 7, pages 1133 - 1142
    - S. M. SCHMUTZ ET AL., "Chromosomal aneuploidy associated with spontaneous abortions and neonatal losses in cattle", J VET DIAGN INVEST, (1996), vol. 8, pages 91 - 95
    - POPESCU, C. P.; BONNEAU, M.; TIXIER, M.; BAHRI, I.; BOSCHER, J., "Reciprocal translocations in pigs", THE JOURNAL OF HEREDITY, (1984), vol. 75, pages 448 - 452
    - LEAR TL; BAILEY E, "Equine clinical cytogenetics: the past and future", CYTOGENET GENOME RES., (2008), vol. 120, no. 1-2, pages 42 - 9
    - HALNAN CR, "Equine cytogenetics: role in equine veterinary practice", EQUINE VET J, (198505), vol. 17, no. 3, pages 173 - 7
    - MATTHEW BREEN, "PhD C.Biol M.I.Biol. Update on Genomics in Veterinary Oncology", TOP COMPANION ANIM MED., (200908), vol. 24, no. 3, pages 113 - 121
    - MATTHEW BREEN, "PhD C.Biol M.I.Biol, Update on Genomics in Veterinary Oncology", TOP COMPANION ANIM MED., (200908), vol. 24, no. 3, pages 113 - 121
    - BREZINA PR ET AL., "Preimplantation Genetic Screening: A Practical Guide", CLIN MED INSIGHTS REPROD HEALTH, (20130227), vol. 7, pages 37 - 42
    - ROBERT G, "EDWARDS. An astonishing journey into reproductive genetics since the 1950's", REPROD. NUTR. DEV., (2005), vol. 45, pages 299 - 306
    - NORBERT GLEICHER ET AL., "Preimplantation genetic screening (PGS) still in search of a clinical application: a systematic review", REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, (2014), vol. 12, doi:doi:10.1186/1477-7827-12-22, page 22, XP021180923

DOI:   http://dx.doi.org/10.1186/1477-7827-12-22
    - MASTENBROEK S; TWISK M; VAN ECHTEN-ARENDS J; SIKKEMA-RADDATZ B; KOREVAAR JC; VERHOEVE HR; VOGEL NE; ARTS EG; DE VRIES JW; BOSSUYT, "In vitro fertilization with preimplantation genetic screening", N ENGL J MED, (2007), vol. 357, pages 9 - 17
    - ANDERSON RA; PICKERING S, "The current status of preimplantation genetic screening: British fertility society policy and practice guidelines", HUM FERTIL (CAMB, (2008), vol. 11, pages 71 - 75
    - GERAEDTS J ET AL., "Polar body array CGH for prediction of the status of the corresponding oocyte", CLINICAL RESULTS
    - AGLI MC ET AL., "Polar body array CGH for prediction of the status of the corresponding oocyte", HUM REPROD., (201108), vol. 16, no. 11, pages 3181 - 85
    - KULIEV A; VERLINSKY Y, "Place of preimplantation genetic diagnosis in genetic practice", AM J MED GENET A, (2005), vol. 134A, pages 105 - 110
    - HARDARSON T; HANSON C; LUDIN K; HILLENSIO T; NILSSON L; STEVIC J; REISMER E; BORG K; WIKLAND M; BERGH C, "Preimplantation genetic screening in women of advanced maternal age causes a decrease in clinical pregnancy rate: a randomized controlled trial", HUM REPROD, (2008), vol. 23, pages 2806 - 2812
    - MAUSUMI DAS, M.D.; HANANEL E. G. HOLZER, M.D., "Recurrent implantation failure: gamete and embryo factors", FERTILITY AND STERILITY, (201205), vol. 97, no. 5
    - RAZIEL A; FRIEDLER S; SCHACHTER M; KASTERSTEIN E; STRASSBURGER D; RON-EI R, "Increased frequency of female partner chromosomal abnormalities in patients with high-order implantation failure after in vitro fertilization", FERTIL STERIL, (2002), vol. 78, pages 515 - 9
    - GINSBURG ES; BAKER VL; RACOWSKY C; WANTMAN E; GOLDFARB J; STERN JE, "Use of preimplantation genetic diagnosis and preimplantation genetic screening in the United States: a Society for Assisted Reproductive Technology Writing Group paper", FERTIL STERIL, (2011), vol. 96, doi:doi:10.1016/j.fertnstert.2011.07.1139, pages 865 - 868, XP028301090

DOI:   http://dx.doi.org/10.1016/j.fertnstert.2011.07.1139
    - BASSEM A. BEJJANI; LISA G. SHAFFER, "Application of Array-Based Comparative Genomic Hybridization to Clinical Diagnostics", JOURNAL OF MOLECULAR DIAGNOSTICS, (200611), vol. 8, no. 5
    - STEPHANIE N. DORMAN ET AL., "Expanding probe repertoire and improving reproducibility in human genomic hybridization", NUCLEIC ACIDS RESEARCH, (2013), vol. 41, no. 7, page E81
    - PINKE,D.; LANDEGENT,J.; COLLINS,C.; FUSCOE,J.; SEGRAVES,R.; LUCAS,J.; GRAY,J., "Fluorescence in situ hybridization with human chromosome specific libraries: detection of trisomy 21 and translocations of chromosome 4", PROC. NATL ACAD. SCI. USA, (1988), vol. 85, pages 9138 - 9142
    - ANDY W PANG, "Towards a comprehensive structural variation map of an individual human genome", GENOME BIOLOGY, (2010), vol. 11, doi:doi:10.1186/gb-2010-11-5-r52, page R52, XP021085607

DOI:   http://dx.doi.org/10.1186/gb-2010-11-5-r52
    - MALCOLM A. FERGUSON-SMITH, "MBChB, FRCPath, FRS. Cytogenetics and the evolution of medical genetics", GENET MED, (2008), vol. 10, no. 8, pages 553 - 559
    - CONRAD,D.F.; PINTO,D.; REDON,R.; FEUK,L.; GOKCUMEN,O.; ZHANG,Y.; AERTS,J.; ANDREWS,T.D.; BARNES,C.; CAMPBELL,P. ET AL., "Origins and functional impact of copy number variation in the human genome", NATURE, (2010), vol. 464, doi:doi:10.1038/nature08516, pages 704 - 712, XP055146767

DOI:   http://dx.doi.org/10.1038/nature08516
    - WELLS D ET AL., "Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH", MOL HUM REPROD., (200812), vol. 14, no. 12, pages 703 - 10
    - VANNESTE E ET AL., "New array approaches to explore single cells genomes", FRONT GENET., (20120327), vol. 3, page 44
    - PINKE,D.; SEGRAVES,R.; SUDAR,D.; CLARK,S.; POOLE,L.; KOWBEL,D.; COLLINS,C.; KUO,W.L.; CHEN,C.; ZHAI,Y. ET AL., "High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays", NAT. GENET., (1998), vol. 20, pages 207 - 211
    - GRAY, J.W.; PINKE,D., "Molecular cytogenetics in human cancer diagnosis", CANCER, (1992), vol. 69, pages 1536 - 1542
    - SHINAWI,M.; CHEUNG,S.W., "The array CGH and its clinical applications", DRUG DISCOV. TODAY, (2008), vol. 13, doi:doi:10.1016/j.drudis.2008.06.007, pages 760 - 770, XP025430476

DOI:   http://dx.doi.org/10.1016/j.drudis.2008.06.007
    - VIKAS BANSAL, "A statistical method for the detection of variants from next-generation resequencing of DNA pools", BIOINFORMATICS, (20100615), vol. 26, no. 12, doi:doi:10.1093/bioinformatics/btq214, pages I318 - I324, XP055259653

DOI:   http://dx.doi.org/10.1093/bioinformatics/btq214
    - JANUS S JAKOBSEN, "Amplification of pico-scale DNA mediated by bacterial carrier DNA for small-cell-number transcription factor ChIP-seq", BMC GENOMICS, (2015), vol. 16, doi:doi:10.1186/s12864-014-1195-4, page 46, XP021212735

DOI:   http://dx.doi.org/10.1186/s12864-014-1195-4
    - SVETLANA A ET AL., "Microarray-Based Comparative Genomic Hybridization Using Sex-Matched Reference DNA Provides Greater Sensitivity for Detection of Sex Chromosome Imbalances than Array-Comparative Genomic Hybridization with Sex-Mismatched Reference", DNA, (200905), vol. 11, no. 3, doi:doi:10.2353/jmoldx.2009.080064, pages 226 - 237, XP055233498

DOI:   http://dx.doi.org/10.2353/jmoldx.2009.080064
    - TINEKE E. BUFFART; DANIELLE ISRAELI; MARIANNE TIJSSEN; SJOERD J. VOSSE; ALAN MR IC; GERRIT A. MEIJER; BAUKE YLSTRA, ACROSS ARRAY COMPARATIVE GENOMIC HYBRIDIZATION: A STRATEGY TO REDUCE REFERENCE CHANNEL HYBRIDIZATIONS, (200811), vol. 47, no. 11, pages 994 - 1004
    - G.L. HARTON ET AL., "ESHRE PGD Consortium/Embryology Special Interest Group-best practice guidelines for polar body and embryo biopsy for preimplantation genetic diagnosis/screening (PGD/PGS", HUMAN REPRODUCTION, (2010), vol. 0, no. 0, pages 1 - 6
    - PRISCILA RAMOS-IBEAS, "An Efficient System to Establish Biopsy-Derived Trophoblastic Cell Lines from Bovine Embryos", BIOLOGY OF REPRODUCTION, (2014), vol. 91, no. 1, pages 15,1 - 10
    - PINTO,D.; DARVISHI,K.; SHI,X.; RAJAN,D.; RIGLER,D.; FITZGERALD,T.; LIONEL,A.C.; THIRUVAHINDRAPURAM,B.; MACDONALD,J.R.; MILLS,R. ET, "Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants", NAT. BIOTECHNOL., (2011), vol. 29, doi:doi:10.1038/nbt.1852, pages 512 - 520, XP002735142

DOI:   http://dx.doi.org/10.1038/nbt.1852
    - DELLINGER,A.E.; SAW,S.-M.; GOH,L.K.; SEIELSTAD,M.; YOUNG,T.L.; LI,Y.-J., "Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays", NUCLEIC ACIDS RES., (2010), vol. 38, page EL05
    - LAI,W.R.; JOHNSON,M.D.; KUCHERLAPATI,R.; PARK,P.J., "Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data", BIOINFORMATICS, (2005), vol. 21, doi:doi:10.1093/bioinformatics/bti611, pages 3763 - 3770, XP055233480

DOI:   http://dx.doi.org/10.1093/bioinformatics/bti611
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.