Pages that link to "Q35759080"
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The following pages link to Concurrent whole-genome haplotyping and copy-number profiling of single cells (Q35759080):
Displaying 27 items.
- Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification. (Q34550417) (← links)
- Mesenchymal stromal cells of osteosarcoma patients do not show evidence of neoplastic changes during long-term culture. (Q35770479) (← links)
- High-Definition Medicine (Q38608277) (← links)
- The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists (Q38852215) (← links)
- Prenatal and pre-implantation genetic diagnosis (Q38954748) (← links)
- How can zygotes segregate entire parental genomes into distinct blastomeres? The zygote metaphase revisited (Q39155966) (← links)
- Karyomapping and how is it improving preimplantation genetics? (Q39274880) (← links)
- Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy (Q41441857) (← links)
- Genome stability of bovine in vivo-conceived cleavage-stage embryos is higher compared to in vitro-produced embryos. (Q47776742) (← links)
- A speculative outlook on embryonic aneuploidy: can molecular pathways be involved? (Q47797736) (← links)
- Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing (Q47869201) (← links)
- Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos (Q48702835) (← links)
- Importance of embryo aneuploidy screening in preimplantation genetic diagnosis for monogenic diseases using the karyomap gene chip (Q49912258) (← links)
- Novel technologies emerging for preimplantation genetic diagnosis and preimplantation genetic testing for aneuploidy. (Q53677632) (← links)
- Detecting mosaicism in trophectoderm biopsies. (Q54032096) (← links)
- Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience. (Q55262442) (← links)
- Recent developments in genetics and medically assisted reproduction: from research to clinical applications (Q56927575) (← links)
- Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M (Q58088123) (← links)
- Long-Read Sequencing Emerging in Medical Genetics (Q64249048) (← links)
- Genotyping single-sperm cells by universal MARSALA enables the acquisition of linkage information for combined pre-implantation genetic diagnosis and genome screening. (Q64940842) (← links)
- scHaplotyper: haplotype construction and visualization for genetic diagnosis using single cell DNA sequencing data (Q89480995) (← links)
- Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA (Q89556540) (← links)
- In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages (Q91106778) (← links)
- High-resolution mapping of reciprocal translocation breakpoints using long-read sequencing (Q92464069) (← links)
- Distinguishing between carrier and noncarrier embryos with the use of long-read sequencing in preimplantation genetic testing for reciprocal translocations (Q92850025) (← links)
- Recent developments in genetics and medically-assisted reproduction: from research to clinical applications†‡ (Q93118941) (← links)
- Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy (Q93200978) (← links)