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Table 1 Comparison of workflows using NGS and aCGH for 24-chromosome copy number analysis

From: Application of next-generation sequencing for 24-chromosome aneuploidy screening of human preimplantation embryos

 

aCGH

NGS

1

Embryo biopsy

NA

Embryo biopsy

2

Sample collection

Reference gDNA (+10 min)

Sample collection

3

WGA (3 hrs)

WGA (3 hrs)

WGA (3 hrs)

4

Labeling of amplified DNA (1 hrs)

Pooling and labeling of amplified DNA (1 hrs)

Qualification and dsDNA input dilution (20 min)

5

Preparation of labeled DNA (1 hrs)

Preparation of labeled DNA (1 hrs)

Tagmentation (20 min)

6

Hybridization to array (2 hrs)

PCR amplification (50 min)

7

Washing and Scanning (20 min)

PCR clean-up (30 min)

8

Cytogenomics analysis (40 min)

Library normalization (30 min)

9

NA

Library pooling and loading (10 min)

10

N/A

Sequencing (6 hrs)

11

N/A

Bioinformatics analysis (2 hrs)

Total hrs

~8 hrs

~14 hrs

  1. NGS: next generation sequencing
  2. aCGH: array comparative genomic hybridization
  3. WGA: whole-genome amplification
  4. NA: not applicable