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Items: 1 to 20 of 810

1.

Genetic alterations crossing the borders of distinct hematopoetic lineages and solid tumors: Diagnostic challenges in the era of high-throughput sequencing in hemato-oncology.

Shumilov E, Flach J, Pabst T, Fiedler M, Angelillo-Scherrer A, Trümper L, Joncourt R, Kohlmann A, Bacher U.

Crit Rev Oncol Hematol. 2018 Jun;126:64-79. doi: 10.1016/j.critrevonc.2018.03.020. Epub 2018 Mar 29. Review.

PMID:
29759569
2.

[Progress in next-generation sequencing research of non-syndromic oral clefts].

Wang MY, Liu DJ, Huang H, Li WY, Zhou R, Zhu HP, Zhou ZB, Wu T.

Zhonghua Liu Xing Bing Xue Za Zhi. 2018 Mar 10;39(3):387-390. doi: 10.3760/cma.j.issn.0254-6450.2018.03.026. Review. Chinese.

PMID:
29609259
3.

Targeted next-generation sequencing of malignant peripheral nerve sheath tumor of the pterygopalatine fossa with intracranial metastatic recurrence.

Bao X, Kong X, Yang C, Wu H, Ma W, Wang R.

Medicine (Baltimore). 2018 Jan;97(4):e9636. doi: 10.1097/MD.0000000000009636. Review.

4.

Recent insights into the tick microbiome gained through next-generation sequencing.

Greay TL, Gofton AW, Paparini A, Ryan UM, Oskam CL, Irwin PJ.

Parasit Vectors. 2018 Jan 4;11(1):12. doi: 10.1186/s13071-017-2550-5. Review.

5.

Implementation of "clinical sequencing" in cancer genome medicine in Japan.

Kohno T.

Cancer Sci. 2018 Mar;109(3):507-512. doi: 10.1111/cas.13486. Epub 2018 Feb 2. Review.

6.

The application of MutMap in forward genetic studies based on whole-genome sequencing.

Yuan JH, Li JH, Yuan JJ, Jia KL, Li SF, Deng CL, Gao WJ.

Yi Chuan. 2017 Dec 20;39(12):1168-1177. doi: 10.16288/j.yczz.17-095. Review.

PMID:
29258987
7.

New monogenic disorders identify more pathways to neutropenia: from the clinic to next-generation sequencing.

Corey SJ, Oyarbide U.

Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):172-180. doi: 10.1182/asheducation-2017.1.172. Review.

8.

Next-generation sequencing: recent applications to the analysis of colorectal cancer.

Del Vecchio F, Mastroiaco V, Di Marco A, Compagnoni C, Capece D, Zazzeroni F, Capalbo C, Alesse E, Tessitore A.

J Transl Med. 2017 Dec 8;15(1):246. doi: 10.1186/s12967-017-1353-y. Review.

9.

The evolving role of genomic testing in assessing prognosis of patients with myelodysplastic syndromes.

Steensma DP.

Best Pract Res Clin Haematol. 2017 Dec;30(4):295-300. doi: 10.1016/j.beha.2017.09.009. Epub 2017 Sep 22. Review.

PMID:
29156198
10.

Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines: A Joint Recommendation of the Association for Molecular Pathology and the College of American Pathologists.

Roy S, Coldren C, Karunamurthy A, Kip NS, Klee EW, Lincoln SE, Leon A, Pullambhatla M, Temple-Smolkin RL, Voelkerding KV, Wang C, Carter AB.

J Mol Diagn. 2018 Jan;20(1):4-27. doi: 10.1016/j.jmoldx.2017.11.003. Epub 2017 Nov 21. Review.

PMID:
29154853
11.

B-cell receptor repertoire sequencing in patients with primary immunodeficiency: a review.

Ghraichy M, Galson JD, Kelly DF, Trück J.

Immunology. 2018 Feb;153(2):145-160. doi: 10.1111/imm.12865. Epub 2017 Dec 18. Review.

PMID:
29140551
12.

Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.

Badeau M, Lindsay C, Blais J, Nshimyumukiza L, Takwoingi Y, Langlois S, Légaré F, Giguère Y, Turgeon AF, Witteman W, Rousseau F.

Cochrane Database Syst Rev. 2017 Nov 10;11:CD011767. doi: 10.1002/14651858.CD011767.pub2. Review.

PMID:
29125628
13.

Genomic Epidemiology of Tuberculosis.

Comas I.

Adv Exp Med Biol. 2017;1019:79-93. doi: 10.1007/978-3-319-64371-7_4. Review.

PMID:
29116630
14.

Methods and novel technology for microRNA quantification in colorectal cancer screening.

Moody L, He H, Pan YX, Chen H.

Clin Epigenetics. 2017 Oct 24;9:119. doi: 10.1186/s13148-017-0420-9. eCollection 2017. Review.

15.

[Clinical Application of NGS-Based Clinical Sequencing].

Nishio K, Sakai K.

Gan To Kagaku Ryoho. 2017 Oct;44(10):813-816. Review. Japanese.

PMID:
29066670
16.

T cell clonality assessment: past, present and future.

Mahe E, Pugh T, Kamel-Reid S.

J Clin Pathol. 2018 Mar;71(3):195-200. doi: 10.1136/jclinpath-2017-204761. Epub 2017 Oct 21. Review. Erratum in: J Clin Pathol. 2018 Jul;71(7):660.

17.

Maximizing ecological and evolutionary insight in bisulfite sequencing data sets.

Lea AJ, Vilgalys TP, Durst PAP, Tung J.

Nat Ecol Evol. 2017 Aug;1(8):1074-1083. doi: 10.1038/s41559-017-0229-0. Epub 2017 Jul 21. Review.

18.

Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis.

Goldfeder RL, Wall DP, Khoury MJ, Ioannidis JPA, Ashley EA.

Am J Epidemiol. 2017 Oct 15;186(8):1000-1009. doi: 10.1093/aje/kww224. Review.

PMID:
29040395
19.

The Role of Next-Generation Sequencing in Sarcomas: Evolution From Light Microscope to Molecular Microscope.

Groisberg R, Roszik J, Conley A, Patel SR, Subbiah V.

Curr Oncol Rep. 2017 Oct 13;19(12):78. doi: 10.1007/s11912-017-0641-2. Review.

PMID:
29030741
20.

Loeffler 4.0: Diagnostic Metagenomics.

Höper D, Wylezich C, Beer M.

Adv Virus Res. 2017;99:17-37. doi: 10.1016/bs.aivir.2017.08.001. Epub 2017 Sep 21. Review.

PMID:
29029726

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