# Why sequence DNA?

## Why do we sequence DNA?

In broad terms there are three things we would like to sequence

• PCR products a.k.a. amplicons
• Random genomic fragments a.k.a shotgun
• RNA messengers

## Amplicons

• highly targeted
• enables analysis of genetic variation in specific regions
• uses primers targeted to regions of interest
• useful for the discovery of mutations in complex samples
• such as tumors mixed with germline DNA
• used in sequencing the 16S rRNA gene in metagenomics

## RNA sequencing

• Reverse transcription into cDNA
• Easier when there is a poly-A tail
• Usually the genome is known, and we care only about measuring gene expression
• If the genome is unknown, the mRNA gives us a good part of the genome
• That strategy is called expressed sequence tags (EST)

In all these cases we get a DNA fragment, about a few thousands bp long (let’s say 500–5000bp)

Each fragment is a physical object

Each strand can be sequenced and produce a read

Usually we have two reads for each fragment

They are sometimes called “forward” and “reverse” reads

# How sequencing works

## DNA sequencing

There are many sequencing methods, based on different physicochemical properties

• activity of restriction enzymes
• florescence
• electronic properties of nucleotides
• chemistry of DNA duplex formation

They are in constant development. We will focus on their key properties

See DNA sequencing on the WikiPedia for more details

• Sanger method: few short reads
• NGS: many very short reads
• 3rd generation: few long reads

## Idea of Sanger method

DNA is separated in 4 parts, each part is mixed with a different restriction enzyme. Then the fragments are separated by electrophoresis.

In a second version, each part is marked with a different fluorophores and then placed in a single capilar electrophoresis, with a light detector

## Cloning vector

• know restriction-enzyme cut sites
• known binding-sites for primers
• antibiotic-resistance genes
• replication origin site

Part of the vector will be sequenced in every read

## Sanger method’s result

The result is a chromatogram. Filenames ending in .AB1 or .SCF

## New generation sequencing

• Roche 454
• Illumina Solexa
• Ion Torrent
• ABI SOLID

Third generation

• DNA nanoball
• Pacific Biotech (PacBio)

## Roche 454

The fragments are then amplified by PCR

Each bead is placed in a single well of a slide

Each well will contain a single bead, covered in many PCR copies of a single sequence

The slide is flooded with one of the four NTP species

## Roche 454

The nucleotide is incorporated when it matches the template

If that single base repeats, then more will be added

The addition of each nucleotide releases a light signal, and is registered with a hight resolution video

## Roche 454

This NTP mix is washed away

The next NTP mix is now added and the process repeated, cycling through the four NTPs.

This kind of sequencing generates graphs for each sequence read, showing the signal density for each nucleotide wash

The sequence can then be determined computationally from the signal density in each wash.

## Roche 454

Sequencing by synthesis

• can sequence 0.7 gigabase per run

• run time 23 hours

## Illumina Solexa

also sequencing by synthesis

• old model Genome Analyzer can sequence 1Gb per run
• Solexa model can sequence 600 Gb per run
• HiSeq model 100 bases read length average 30Gb per run
• 11 day in regular mode
• 2 day in rapid run mode

## Illumina Solexa

over 70% of the market

• ∼$1000 MiSeq • ∼$3000 HighSeq
• ∼ 1.5 days

## Illumina Solexa

• output of sequencing data per run: 600 Gb
• read lengths: approximately 100 bp
• cost is cheap
• run times are long: 3-10 days

## ABI-SOLID

Sequencing by ligation

Supported Oligonucleotide Ligation and Detection (SOLiD)

• Solid 4 model can read 80-100 Gb per run (coverage 30Gb)
• average read length 50 bases
• fragment length 400-600-bp

## ABI-SOLID

The advantage of this method is accuracy with each base interrogated twice

• short read lengths (50–75 bp)
• very long run times of 7 to 14 days
• need for computational infrastructure and expert computing personnel for analysis of the raw data

## Ion torrent

• Developed by the inventors of 454 sequencing
• With two major changes.
• nucleotide sequences are detected electronically by changes in the pH of the surrounding solution rather than by the generation of light
• sequencing reaction is performed in a microchip with flow cells and electronic sensors on each cell
• The incorporated nucleotide is converted to an electronic signal

## PacBio

• PacBio model RS II produces average read lengths over 10 kb, with an N50 of more than 20 kb and maximum read lengths over 60 kb
• Error rate of a continuous long read is relatively high (around 11%–15%)
• The error rate can be reduced by generating circular consensus sequences reads with sufficient sequencing passes.

## Summary

Method Read length (bp) Error rate (%) No. of reads per run Time per run Cost per million bases (USD)
Sanger ABI 3730x1 600-1000 0.001 96 0.5–3 h 500
Illumina HiSeq 2500 2 × 250 0.1 1.2 × 109 (pairs) 1–6 days 0.04
PacBio RS II: P6-C4 1.0–1.5×104 13 3.5–7.5 × 104 0.5–4 h 0.4–0.8
Oxford Nanopore MinION 2–5 × 103 38 1.1–4.7 × 104 50 h 6.44–17.9