whole genome sequencing new and its types including shortgun and clone by clone

401 views 15 slides Apr 11, 2024
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About This Presentation

whole genome sequencing and its methods
types of whole genome sequencing -
1 clone by clone sequencing
2 short gun sequencing


Slide Content

WHOLE GENOME SEQUENCING BY GAURISHA SHARMA

INTRODUCTION HISTORY WORKFLOW OF WGS SHORTGUN SEQUENCING CLONE BY CLONE SEQUENCING ADVANTAGES AND DISADVANTAGES INDEX

WHOLE GENOME SEQUENCING All genome has unique genetic code or genome that is composed of bases ( A,T,C,G). WGS ia an invitro technique which is used to determine the nucleotide sequence of the genome of that organism . Whole-genome sequencing  is a process that determines the DNA sequence of an entire genome.

In 1977, Sanger also used his method to sequence the first ever complete genome: the one of the bacteriophage PhiX174 (virus that infects  E. coli ). Also in 1977, Maxam and Gilbert introduced a method for DNA sequencing that was based on chemical modification of DNA. The WGS is invented by the J. craig venter and H. smith in 1995.  History

The whole genome sequencing comprises of various steps to sequence the whole genome . Firstly the DNA is cutted into several pieces using different techniques . Then the fregmented pieces of DNA is ligated into the plasmid. then the plasmid contaning the desired fragment of DNA is inserted into the Ecoli . Micro titer plates containing the ecoli is heated to 95 degree C for the separation of the plasmid and release of the DNA. Now the DNA fragments are amplified Workflow of WGS

The amplified DNA attracted towards the carboxyl coated magnatic beads, These beads help in the purification and sepration of the dna for the preparation of DNA library The DNA library is prepared and the small DNA tags or barcodes are added to the DNA contigs which will help in the identification of the DNA . The refered genome is added to the sequencer according to which the DNA assambles and sequenced The DNA sequences is done.

The short gun sequencing is used for the sequencing of long DNA strands Dna is broken up randomly into the numerous small segments, which are sequenced by the chain termination method. Multiple overlapping reds for the target DNA are obtained by performing the several rounds of this fragmentation and sequencing. Computer program then use overlapping ends of the different reads to assemble them into continuous sequence. Short gun sequencing

These analysis method involved can be time consuming and computationally heavy often requiring complex and expensive infrastructures. Limitation

The method preferred by the human genome project is the hierarchical shotgun sequencing method. Also known as the clone by clone sequencing The map based method top down sequencing Clone by clone sequencing

The genome is split into larger fragments ( 50-200kb) using restricted cutting enzymes that contains a known marker. These fragments are closed in bacteria ( e.coli ) using BACs where they replicated and stored. The BACs inserts are isolated and the whole genome is mapped by markers. The fragments contained in these clones have different ends. Each BACs fragments is fragmented randomly into smaller pieces and these fragments are individually sequenced using the automated Sanger sequencing. These sequences are aligned so that identical sequences are overlapping. The assembly of the genome is done on the basis of prior knowledge of the marker used to localize sequenced fragments to their genomic location. Steps

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Requires relatively large amount of highly pure DNA. Its expensive Time consuming Limitation

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