Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
about
Whole genome sequence analysis of BT-474 using complete Genomics' standard and long fragment read technologies.Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes.High mutational rates of large-scale duplication and deletion in Daphnia pulex.Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analysesPremalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies.Evidence for feasibility of fetal trophoblastic cell-based noninvasive prenatal testing.Using fetal cells for prenatal diagnosis: History and recent progress.The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologistsPrenatal and pre-implantation genetic diagnosis.Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular Haplotyping.InPhaDel: integrative shotgun and proximity-ligation sequencing to phase deletions with single nucleotide polymorphismsWhole genome prediction for preimplantation genetic diagnosis.Pure CTCs, advanced WGS, and precise personalized combination therapies.Haplotype phasing of whole human genomes using bead-based barcode partitioning in a single tube.Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non-invasive prenatal testing.Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos.Novel technologies emerging for preimplantation genetic diagnosis and preimplantation genetic testing for aneuploidy.
P2860
Q35920454-DE7B22CB-EB66-44A4-A60D-15FCF079CEF2Q36021845-D87383AD-A7A0-425D-ABE3-921244B9D784Q36159921-944620D5-8863-413A-B9BF-DDC18A3FA54CQ36406085-AAFCDCA5-FFFD-4F9D-8C43-83877546DE34Q36435251-F734435E-09DA-4610-A63F-CEE4BF41A4B8Q37221493-10C0E786-7ADE-4457-981A-87A55037BA42Q37456619-56F0D939-1276-4E7A-919F-F670A760F6C2Q38822505-529B044A-A359-4F4C-9A81-75C7CE8152CCQ38852215-D5449712-159E-4878-9C31-1EBE0DDC4730Q38954748-73BAFE44-60B4-4001-8BAD-BBD8DA24D55FQ38990647-1AF4EA4A-37C2-4D8B-BED7-6F0E3F66BFD6Q39829557-2F698BF5-FB53-4E64-A2F0-2B4C3CAF47EDQ41170203-FD31DF14-E568-47C9-98C7-8A13170A1198Q42364952-BE53D3FF-17BD-4869-9994-88654F1CDD7AQ45978724-3E6131E0-48A4-4C01-819C-626FEF98373FQ47586484-82B9B906-AF70-4749-AFF8-2CAA72B4CB5AQ48702835-BDA8FBC3-A163-4340-B688-30ACF2BB4FF6Q53677632-EF3B3D40-907D-4C63-B9FB-FC8A8AB3532E
P2860
Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
description
2015 nî lūn-bûn
@nan
2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Detection and phasing of singl ...... vanced whole-genome sequencing
@ast
Detection and phasing of singl ...... vanced whole-genome sequencing
@en
type
label
Detection and phasing of singl ...... vanced whole-genome sequencing
@ast
Detection and phasing of singl ...... vanced whole-genome sequencing
@en
prefLabel
Detection and phasing of singl ...... vanced whole-genome sequencing
@ast
Detection and phasing of singl ...... vanced whole-genome sequencing
@en
P2093
P2860
P356
P1433
P1476
Detection and phasing of singl ...... vanced whole-genome sequencing
@en
P2093
Alan Berkeley
Bahram G Kermani
Birgit Crain
Daniel M Hayden
Mark A McElwain
Misha R Agarwal
Natali Gulbahce
Oleg Alferov
Radoje Drmanac
Rebecca Yu Zhang
P2860
P304
P356
10.1101/GR.181255.114
P577
2015-02-11T00:00:00Z