[HTML][HTML] Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck, T Sante… - Fertility and sterility, 2015 - Elsevier
Objective To add evidence that massive parallel sequencing (MPS) is a valuable substitute
for array comparative genomic hybridization (arrayCGH) with a resolution that is more …

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck… - Fertility and …, 2015 - pubmed.ncbi.nlm.nih.gov
Objective To add evidence that massive parallel sequencing (MPS) is a valuable substitute
for array comparative genomic hybridization (arrayCGH) with a resolution that is more …

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts.

L Deleye, A Dheedene, D De Coninck, T Sante… - Fertility and …, 2015 - europepmc.org
Shallow whole genome sequencing is well suited for the detection of chromosomal
aberrations in human blastocysts. - Abstract - Europe PMC Sign in | Create an account https://orcid.org …

[PDF][PDF] Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck… - IRU YDULDQW …, 2015 - biblio.ugent.be
Objective: To add evidence that massive parallel sequencing (MPS) is a valuable substitute
for array comparative genomic hybridization (arrayCGH) with a resolution that is more …

[引用][C] Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck, T Sante… - Fertility and …, 2015 - cir.nii.ac.jp
Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations
in human blastocysts | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細 …

[PDF][PDF] Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck, T Sante… - Fertility and …, 2015 - researchgate.net
Objective: To add evidence that massive parallel sequencing (MPS) is a valuable substitute
for array comparative genomic hybridization (arrayCGH) with a resolution that is more …

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck, T Sante… - Fertility and …, 2015 - infona.pl
To add evidence that massive parallel sequencing (MPS) is a valuable substitute for array
comparative genomic hybridization (arrayCGH) with a resolution that is more appropriate for …

[PDF][PDF] Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck, T Sante… - Fertility and …, 2015 - academia.edu
Objective: To add evidence that massive parallel sequencing (MPS) is a valuable substitute
for array comparative genomic hybridization (arrayCGH) with a resolution that is more …

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck, T Sante… - Fertility and …, 2015 - fertstert.org
Objective To add evidence that massive parallel sequencing (MPS) is a valuable substitute
for array comparative genomic hybridization (arrayCGH) with a resolution that is more …

[引用][C] Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

L Deleye, A Dheedene, D De Coninck… - FERTILITY AND …, 2015 - biblio.ugent.be
Keywords preimplantation genetic diagnosis, chromosomal rearrangement, Massive parallel
sequencing, blastocyst biopsy, whole genome amplification, RANDOMIZED CONTROLLED …