Preparation of DNA libraries for NGS
Next Generation Sequencing (NGS) requires careful preparation of the genetic material prior to the sequencing reaction to ensure reliable results.
The preparation of DNA banks is composed of 4 main steps whose sequence may vary depending on the methods used:
1. Fragmentation
DNA is fragmented either enzymatically or by sonication to create small random fragments.
2. End repair
Since DNA fragmentation does not result in homogeneous, open-ended fragments, end repair is necessary to ensure that each molecule is free of overhangs and contains 5' phosphate and 3' hydroxyl groups.
3. Binding of adapters
The adapters (small sequences of double-stranded synthetic DNA) are then bound to these fragments with the help of a DNA ligase. The adaptors allow the sequence to bind to the support but also to identify the sample analyzed thanks to the indexes. The adapters contain motifs necessary for the following steps (clonal amplification and sequencing)
4. Amplification of the bank
Amplification of the bank is necessary so that the signal received by the sequencer is strong enough to be detected accurately.
