Journal of Next Generation Sequencing & Applications

An Inherited Arrhythmia Syndrome with Long QT, Sudden Death and Depolarization Disorder Due to an In-Frame Deletion in Exon 16 of the CACNA1C Gene

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000144 ◽

2017 ◽

Vol 04 (01) ◽

Author(s):

Muhammad Arshad Rafiq ◽

Tamara T Koopmann ◽

Laura A Zahavich ◽

Meena Fatah ◽

Robert M Hamilton

Keyword(s):

Sudden Death ◽

Long Qt ◽

Inherited Arrhythmia

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Next-generation Sequencing in the Clinical Decision Making in Hypertrophic Cardiomyopathy

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000145 ◽

2017 ◽

Vol 04 (01) ◽

Author(s):

Viktor J Horvath ◽

Kristof Arvai ◽

Janos P Kosa ◽

Bernadett Balla ◽

Balint Tobias ◽

...

Keyword(s):

Decision Making ◽

Next Generation Sequencing ◽

Hypertrophic Cardiomyopathy ◽

Clinical Decision Making ◽

Clinical Decision ◽

Next Generation ◽

Generation Sequencing

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Public Databases of 16s rRNA: A Current Perspective and Future Implications

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000151 ◽

2017 ◽

Vol 04 (03) ◽

Author(s):

Vandana Singh ◽

Kunal Maniar ◽

Rajasri Bhattacharayya ◽

Dibyajyoti Banerjee

Keyword(s):

16S Rrna ◽

Current Perspective ◽

A Current

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Next-Generation Sequencing (NGS)-Based Clinical Testing is Recommended for the Detection of Gene Mutations Associated with Familial Myelodysplastic Syndrome and Acute Myeloid Leukemia Predisposition Syndromes

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000153 ◽

2017 ◽

Vol 04 (03) ◽

Author(s):

Ryan S Robetorye

Keyword(s):

Acute Myeloid Leukemia ◽

Next Generation Sequencing ◽

Myelodysplastic Syndrome ◽

Myeloid Leukemia ◽

Gene Mutations ◽

Clinical Testing ◽

Next Generation ◽

Next Generation Sequencing Ngs ◽

Generation Sequencing ◽

Acute Myeloid

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Identification of human genes and its genomics functions via miRNAs of C. elegans on bioinformatics platforms

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000150 ◽

2017 ◽

Vol 04 (02) ◽

Author(s):

Shashi Prabha Agrawal ◽

Mrityunjay Kumar Sinha ◽

Rajnish Kumar

Keyword(s):

C Elegans ◽

Human Genes

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In Silico Identification of B-Cell Epitopes of Leishmania infantum Recombinant Histone Shared with Human Sera Stably Living in Area Where Leishmania Species Does Perpetuate

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000146 ◽

2017 ◽

Vol 04 (01) ◽

Author(s):

Sami Lakhal ◽

Malcolm S Duthie

Keyword(s):

B Cell ◽

In Silico ◽

Leishmania Infantum ◽

Leishmania Species ◽

B Cell Epitopes ◽

Human Sera ◽

In Silico Identification

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The Resilience of Microbial Community Involved in Coking Wastewater Treatment System

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000142 ◽

2017 ◽

Vol 04 (01) ◽

Author(s):

Shang Zhu ◽

Haizhen Wu ◽

Lin Zhou ◽

Chaohai Wei

Keyword(s):

Wastewater Treatment ◽

Microbial Community ◽

Treatment System ◽

Coking Wastewater ◽

Wastewater Treatment System

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KDR Mutation: A High-Frequency Rare Mutation and its Correlation with other Somatic Mutations in Indian Colorectal Cancer Patients

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000148 ◽

2017 ◽

Vol 04 (02) ◽

Cited By ~ 1

Author(s):

Mayank Jauhri ◽

Vani Gupta ◽

Yogender Shokeen ◽

Sachin Minhas ◽

Sunita Bhalla ◽

...

Keyword(s):

Colorectal Cancer ◽

Cancer Patients ◽

High Frequency ◽

Somatic Mutations ◽

Kdr Mutation ◽

Rare Mutation ◽

Colorectal Cancer Patients

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Integrating Next Generation Sequencing, Bioinformatics and Cytogenomics in the Study of Brazilian Mammals

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000147 ◽

2017 ◽

Vol 04 (02) ◽

Author(s):

Naiara Pereira Araujo ◽

Gustavo Campos Silva Kuhn ◽

Marta Svartman

Keyword(s):

Next Generation Sequencing ◽

Next Generation ◽

Generation Sequencing

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Clear Cell Adenocarcinoma of the Colon in the Setting of Attenuated Familial Polyposis: A Rare Variant of Primary Colonic Adenocarcinoma

Journal of Next Generation Sequencing & Applications ◽

10.4172/2469-9853.1000143 ◽

2017 ◽

Vol 04 (01) ◽

Author(s):

Nozha Mhamdi ◽

Ahlem Bdioui ◽

Nihed Abdessayed ◽

Sarra Mestiri ◽

Marwa Guerfela ◽

...

Keyword(s):

Rare Variant ◽

Familial Polyposis ◽

Clear Cell ◽

Clear Cell Adenocarcinoma ◽

Colonic Adenocarcinoma ◽

Adenocarcinoma Of The Colon

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Journal of Next Generation Sequencing & Applications
Latest Publications

TOTAL DOCUMENTS

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Published By Omics Publishing Group

An Inherited Arrhythmia Syndrome with Long QT, Sudden Death and Depolarization Disorder Due to an In-Frame Deletion in Exon 16 of the CACNA1C Gene

Next-generation Sequencing in the Clinical Decision Making in Hypertrophic Cardiomyopathy

Public Databases of 16s rRNA: A Current Perspective and Future Implications

Next-Generation Sequencing (NGS)-Based Clinical Testing is Recommended for the Detection of Gene Mutations Associated with Familial Myelodysplastic Syndrome and Acute Myeloid Leukemia Predisposition Syndromes

Identification of human genes and its genomics functions via miRNAs of C. elegans on bioinformatics platforms

In Silico Identification of B-Cell Epitopes of Leishmania infantum Recombinant Histone Shared with Human Sera Stably Living in Area Where Leishmania Species Does Perpetuate

The Resilience of Microbial Community Involved in Coking Wastewater Treatment System

KDR Mutation: A High-Frequency Rare Mutation and its Correlation with other Somatic Mutations in Indian Colorectal Cancer Patients

Integrating Next Generation Sequencing, Bioinformatics and Cytogenomics in the Study of Brazilian Mammals

Clear Cell Adenocarcinoma of the Colon in the Setting of Attenuated Familial Polyposis: A Rare Variant of Primary Colonic Adenocarcinoma

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Journal of Next Generation Sequencing & ApplicationsLatest Publications

TOTAL DOCUMENTS

H-INDEX

Published By Omics Publishing Group

An Inherited Arrhythmia Syndrome with Long QT, Sudden Death and Depolarization Disorder Due to an In-Frame Deletion in Exon 16 of the CACNA1C Gene

Next-generation Sequencing in the Clinical Decision Making in Hypertrophic Cardiomyopathy

Public Databases of 16s rRNA: A Current Perspective and Future Implications

Next-Generation Sequencing (NGS)-Based Clinical Testing is Recommended for the Detection of Gene Mutations Associated with Familial Myelodysplastic Syndrome and Acute Myeloid Leukemia Predisposition Syndromes

Identification of human genes and its genomics functions via miRNAs of C. elegans on bioinformatics platforms

In Silico Identification of B-Cell Epitopes of Leishmania infantum Recombinant Histone Shared with Human Sera Stably Living in Area Where Leishmania Species Does Perpetuate

The Resilience of Microbial Community Involved in Coking Wastewater Treatment System

KDR Mutation: A High-Frequency Rare Mutation and its Correlation with other Somatic Mutations in Indian Colorectal Cancer Patients

Integrating Next Generation Sequencing, Bioinformatics and Cytogenomics in the Study of Brazilian Mammals

Clear Cell Adenocarcinoma of the Colon in the Setting of Attenuated Familial Polyposis: A Rare Variant of Primary Colonic Adenocarcinoma

Journal of Next Generation Sequencing & Applications
Latest Publications