These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 29374225)

  • 1. Long range haplotyping of paired-homologous chromosomes by single-chromosome sequencing of a single cell.
    Luo D; Zhang M; Liu T; Cao W; Guo J; Mao C; Li Y; Wang J; Huang W; Lu D; Zhang S; Li Z; He J
    Sci Rep; 2018 Jan; 8(1):1640. PubMed ID: 29374225
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-genome haplotyping by dilution, amplification, and sequencing.
    Kaper F; Swamy S; Klotzle B; Munchel S; Cottrell J; Bibikova M; Chuang HY; Kruglyak S; Ronaghi M; Eberle MA; Fan JB
    Proc Natl Acad Sci U S A; 2013 Apr; 110(14):5552-7. PubMed ID: 23509297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ultraaccurate genome sequencing and haplotyping of single human cells.
    Chu WK; Edge P; Lee HS; Bansal V; Bafna V; Huang X; Zhang K
    Proc Natl Acad Sci U S A; 2017 Nov; 114(47):12512-12517. PubMed ID: 29078313
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dense and accurate whole-chromosome haplotyping of individual genomes.
    Porubsky D; Garg S; Sanders AD; Korbel JO; Guryev V; Lansdorp PM; Marschall T
    Nat Commun; 2017 Nov; 8(1):1293. PubMed ID: 29101320
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Oligonucleotide arrays vs. metaphase-comparative genomic hybridisation and BAC arrays for single-cell analysis: first applications to preimplantation genetic diagnosis for Robertsonian translocation carriers.
    Ramos L; del Rey J; Daina G; García-Aragonés M; Armengol L; Fernandez-Encinas A; Parriego M; Boada M; Martinez-Passarell O; Martorell MR; Casagran O; Benet J; Navarro J
    PLoS One; 2014; 9(11):e113223. PubMed ID: 25415307
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Concurrent whole-genome haplotyping and copy-number profiling of single cells.
    Zamani Esteki M; Dimitriadou E; Mateiu L; Melotte C; Van der Aa N; Kumar P; Das R; Theunis K; Cheng J; Legius E; Moreau Y; Debrock S; D'Hooghe T; Verdyck P; De Rycke M; Sermon K; Vermeesch JR; Voet T
    Am J Hum Genet; 2015 Jun; 96(6):894-912. PubMed ID: 25983246
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-genome molecular haplotyping of single cells.
    Fan HC; Wang J; Potanina A; Quake SR
    Nat Biotechnol; 2011 Jan; 29(1):51-7. PubMed ID: 21170043
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Direct chromosome-length haplotyping by single-cell sequencing.
    Porubský D; Sanders AD; van Wietmarschen N; Falconer E; Hills M; Spierings DC; Bevova MR; Guryev V; Lansdorp PM
    Genome Res; 2016 Nov; 26(11):1565-1574. PubMed ID: 27646535
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts.
    Deleye L; Dheedene A; De Coninck D; Sante T; Christodoulou C; Heindryckx B; Van den Abbeel E; De Sutter P; Deforce D; Menten B; Van Nieuwerburgh F
    Fertil Steril; 2015 Nov; 104(5):1276-85.e1. PubMed ID: 26282994
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells.
    Peters BA; Kermani BG; Sparks AB; Alferov O; Hong P; Alexeev A; Jiang Y; Dahl F; Tang YT; Haas J; Robasky K; Zaranek AW; Lee JH; Ball MP; Peterson JE; Perazich H; Yeung G; Liu J; Chen L; Kennemer MI; Pothuraju K; Konvicka K; Tsoupko-Sitnikov M; Pant KP; Ebert JC; Nilsen GB; Baccash J; Halpern AL; Church GM; Drmanac R
    Nature; 2012 Jul; 487(7406):190-5. PubMed ID: 22785314
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple displacement amplification of the DNA from single flow-sorted plant chromosome.
    Cápal P; Blavet N; Vrána J; Kubaláková M; Doležel J
    Plant J; 2015 Nov; 84(4):838-44. PubMed ID: 26400218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs.
    Sanders AD; Falconer E; Hills M; Spierings DCJ; Lansdorp PM
    Nat Protoc; 2017 Jun; 12(6):1151-1176. PubMed ID: 28492527
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Fosmid Pool-Based Next Generation Sequencing Approach to Haplotype-Resolve Whole Genomes.
    Suk EK; Schulz S; Mentrup B; Huebsch T; Duitama J; Hoehe MR
    Methods Mol Biol; 2017; 1551():223-269. PubMed ID: 28138850
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Determination of complete chromosomal haplotypes by bulk DNA sequencing.
    Tourdot RW; Brunette GJ; Pinto RA; Zhang CZ
    Genome Biol; 2021 May; 22(1):139. PubMed ID: 33957932
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].
    Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC
    Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos.
    Dimitriadou E; Melotte C; Debrock S; Esteki MZ; Dierickx K; Voet T; Devriendt K; de Ravel T; Legius E; Peeraer K; Meuleman C; Vermeesch JR
    Hum Reprod; 2017 Mar; 32(3):687-697. PubMed ID: 28158716
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers.
    Zhang S; Lei C; Wu J; Zhou J; Sun H; Fu J; Sun Y; Sun X; Lu D; Zhang Y
    BMC Med Genomics; 2017 Oct; 10(1):60. PubMed ID: 29041973
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Painting of defined chromosomal regions by in situ suppression hybridization of libraries from laser-microdissected chromosomes.
    Lengauer C; Eckelt A; Weith A; Endlich N; Ponelies N; Lichter P; Greulich KO; Cremer T
    Cytogenet Cell Genet; 1991; 56(1):27-30. PubMed ID: 2004552
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Massively parallel sequencing on human cleavage-stage embryos to detect chromosomal abnormality.
    Zhou Z; Ma Y; Li Q; Zhang Y; Huang Y; Tu Z; Ma N; Li M; Wang J; Li J; Lu W
    Eur J Med Genet; 2018 Jan; 61(1):34-42. PubMed ID: 29032163
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Experimental method for haplotype phasing across the entire length of chromosome 21 in trisomy 21 cells using a chromosome elimination technique.
    Wakita S; Hara M; Kitabatake Y; Kawatani K; Kurahashi H; Hashizume R
    J Hum Genet; 2022 Oct; 67(10):565-572. PubMed ID: 35637312
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.