JP2014535050A5 - - Google Patents

Download PDF

Info

Publication number
JP2014535050A5
JP2014535050A5 JP2014537743A JP2014537743A JP2014535050A5 JP 2014535050 A5 JP2014535050 A5 JP 2014535050A5 JP 2014537743 A JP2014537743 A JP 2014537743A JP 2014537743 A JP2014537743 A JP 2014537743A JP 2014535050 A5 JP2014535050 A5 JP 2014535050A5
Authority
JP
Japan
Prior art keywords
probe
short
sequence
long
genomic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2014537743A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014535050A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2012/002423 external-priority patent/WO2013064896A1/en
Publication of JP2014535050A publication Critical patent/JP2014535050A/ja
Publication of JP2014535050A5 publication Critical patent/JP2014535050A5/ja
Pending legal-status Critical Current

Links

JP2014537743A 2011-10-31 2012-10-30 生体試料におけるゲノム再編成を特定又は検出する方法 Pending JP2014535050A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161553889P 2011-10-31 2011-10-31
US61/553,889 2011-10-31
PCT/IB2012/002423 WO2013064896A1 (en) 2011-10-31 2012-10-30 Method for identifying or detecting genomic rearrangements in a biological sample

Publications (2)

Publication Number Publication Date
JP2014535050A JP2014535050A (ja) 2014-12-25
JP2014535050A5 true JP2014535050A5 (https=) 2016-08-18

Family

ID=47559567

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014537743A Pending JP2014535050A (ja) 2011-10-31 2012-10-30 生体試料におけるゲノム再編成を特定又は検出する方法

Country Status (4)

Country Link
US (3) US9133514B2 (https=)
EP (1) EP2773770A1 (https=)
JP (1) JP2014535050A (https=)
WO (1) WO2013064896A1 (https=)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013064895A1 (en) * 2011-10-31 2013-05-10 Genomic Vision Methods for the detection, visualization and high resolution physical mapping of genomic rearrangements in breast and ovarian cancer genes and loci brca1 and brca2 using genomic morse code in conjunction with molecular combing
WO2016077750A1 (en) * 2014-11-14 2016-05-19 Athena Diagnostics, Inc. Methods to detect a silent carrier genotype
CN110199031A (zh) * 2016-11-29 2019-09-03 基因组影像公司 设计用于分析感兴趣的遗传区域中的特定事件的一组多核苷酸序列的方法
EP3887552A1 (en) 2018-11-30 2021-10-06 Genomic Vision Association between integration of viral as hpv or hiv genomes and the severity and/or clinical outcome of disorders as hpv associated cervical lesions or aids pathology

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2755149B1 (fr) * 1996-10-30 1999-01-15 Pasteur Institut Procede de diagnostic de maladies genetiques par peignage moleculaire et coffret de diagnostic
US6828097B1 (en) 2000-05-16 2004-12-07 The Childrens Mercy Hospital Single copy genomic hybridization probes and method of generating same
US20030017159A1 (en) * 2001-05-02 2003-01-23 Jerome Ritz Immunogenic tumor antigens: nucleic acids and polypeptides encoding the same and methods of use thereof
WO2005123961A2 (en) * 2004-06-14 2005-12-29 Ambry Genetics Corporation Approaches to identifying mutations associated with hereditary nonpolyposis colorectal cancer
US7985542B2 (en) * 2006-09-07 2011-07-26 Institut Pasteur Genomic morse code
JP2013524806A (ja) * 2010-04-23 2013-06-20 ゲノミク ビジョン 分子コーミングを用いるゲノムｄｎａ及び感染性ウイルスｄｎａの検出によるウイルス感染の診断

Similar Documents

Publication Publication Date Title
Del Vecchio et al. Next-generation sequencing: recent applications to the analysis of colorectal cancer
Dalgliesh et al. Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes
Stange et al. Expression of an ASCL2 related stem cell signature and IGF2 in colorectal cancer liver metastases with 11p15. 5 gain
JP6700333B2 (ja) ヘテロ接合性の消失（ｌｏｓｓ ｏｆ ｈｅｔｅｒｏｚｙｇｏｓｉｔｙ）を評価するための方法および材料
Shibata et al. Exploration of liver cancer genomes
JP5843840B2 (ja) 新しい癌マーカー
Walker et al. Intraclonal heterogeneity and distinct molecular mechanisms characterize the development of t (4; 14) and t (11; 14) myeloma
Jiang et al. Re-evaluation of the carcinogenic significance of hepatitis B virus integration in hepatocarcinogenesis
Lu et al. Amplification and overexpression of Hsa-miR-30b, Hsa-miR-30d and KHDRBS3 at 8q24. 22-q24. 23 in medulloblastoma
Sutton et al. Targeted next-generation sequencing in chronic lymphocytic leukemia: a high-throughput yet tailored approach will facilitate implementation in a clinical setting
Pitkänen et al. Frequent L1 retrotranspositions originating from TTC28 in colorectal cancer
JP6709541B2 (ja) 大腸癌に対する薬物療法の感受性を予測する方法
JP2021535489A5 (https=)
Iwakawa et al. MYC amplification as a prognostic marker of early-stage lung adenocarcinoma identified by whole genome copy number analysis
Lionetti et al. A compendium of DIS3 mutations and associated transcriptional signatures in plasma cell dyscrasias
JP2017523810A5 (https=)
Sun et al. Extrachromosomal circular DNAs are common and functional in esophageal squamous cell carcinoma
JP2012526563A5 (https=)
JP2014502155A (ja) 癌関連の遺伝子または分子異常の検出
Onsongo et al. CNV-RF is a random forest–based copy number variation detection method using next-generation sequencing
JP2012503985A5 (https=)
Berg et al. Genomic and prognostic heterogeneity among RAS/BRAF V600E/TP53 co‐mutated resectable colorectal liver metastases
JP2014535050A5 (https=)
JP2019514344A (ja) 癌のエピジェネティックプロファイリング
Zhu et al. A systematic analysis on DNA methylation and the expression of both mRNA and microRNA in bladder cancer