Semantic Scholar Open Access 2022 8 sitasi

Different DNA Sequencing Using DNA Graphs: A Study

A. Alanazi G. Muhiuddin Doha A. Al-Balawi Sovan Samanta

Abstrak

Natural genetic material may shed light on gene expression mechanisms and aid in the detection of genetic disorders. Single Nucleotide Polymorphism (SNP), small insertions and deletions (indels), and major chromosomal anomalies are all chromosomal abnormality-related disorders. As a result, several methods have been applied to analyze DNA sequences, which constitutes one of the most critical aspects of biological research. Thus, numerous mathematical and algorithmic contributions have been made to DNA analysis and computing. Cost minimization, deployment, and sensitivity analysis to many factors are all components of sequencing platforms built on a quantitative framework and their operating mechanisms. This study aims to investigate the role of DNA sequencing and its representation in the form of graphs in the analysis of different diseases by means of DNA sequencing.

Penulis (4)

A

A. Alanazi

G

G. Muhiuddin

D

Doha A. Al-Balawi

S

Sovan Samanta

Format Sitasi

Alanazi, A., Muhiuddin, G., Al-Balawi, D.A., Samanta, S. (2022). Different DNA Sequencing Using DNA Graphs: A Study. https://doi.org/10.3390/app12115414

Akses Cepat

Lihat di Sumber doi.org/10.3390/app12115414
Informasi Jurnal
Tahun Terbit
2022
Bahasa
en
Total Sitasi
Sumber Database
Semantic Scholar
DOI
10.3390/app12115414
Akses
Open Access ✓