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Call For Abstract |Next Generation Sequencing Conferences | Meetings International | 2018 | 2019

Annual Next Generation Sequencing & Clinical Diagnostics Congress

Chicago, USA   September 17-18, 2018

Call for Abstract

Shotgun Sequencing expects to grouping a clone longer than the normal read length, it is conceivable to utilize a shotgun approach. The thought is to give the DNA arrangement peruses to such an extent that they cover, and when gathered, yield the entire succession of the clone. 

Transcriptome sequencing essentially focusses on real colleges, establishments, social orders and even huge market in Transcriptome innovation. Transcriptomics is the subject to be centered similarly around both scholarly world and additionally business. It would be gainful for all analysts and understudies who truly need their plans to be actualized essentially. Indeed, even those researchers who will get some business for their examination, this meeting is a noteworthy stage.

 

This method focusses on sequencing all the protein-coding genes within a genome.  It is essential in the study of rare Mendelian diseases, as it involves the identification of genetic variants in each of the individual's genes. The aim of organizing Next Generation Sequencing Conference is to supply exposure to technologies and international tie-ups and to supply data regarding recent trends in sequencing.

 

According to Next Generation Sequencing Meeting discussions, the hybrid sequencing methods utilizes the high-throughput and high-accuracy short read data for correcting errors in the longer reads. This found to reduce the required amount of costlier long-read sequence data and also leads to more complete assemblies including the repetitive regions.

 

Recently the high-throughput-next generation sequencing (HT-NGS) technologies are the most emerging topic in the field of human and animals genomics studies, which is said to produce about 100 times more data compared to that of the most refined capillary sequencers based on the Sanger technique.

 

Cell and gene therapies propose unique opportunities to develop new therapeutic methodologies to treat and potentially cure numerous diseases. This approach provides a widespread resource for  gene transfer, control and silencing including use of cells as gene therapy vehicles. In Next Generation Sequencing Meeting , researchers exchange the information and their research experiences.

 

Analysis of Next-generation sequencing (NGS) data set is a massive challenge. It needs a efficient and intellectual approach to process the NGS data efficiently. Our analysis process includes data quality assessment, comprehensive analysis, interpreting results, and communicating and presenting results to the customers in meaningful formats. The analysis process may also include development of algorithm for some special projects.

 

Next-generation sequencing (NGS) tools comprising of DNA sequencing as well as RNA sequencing provides “omics” methodologies to expose genomic, transcriptomic, and epigenomic landscapes of individual cancers. A collection of genomic aberrations can also be screened simultaneously, such as collective and rare variants, structural variations (e.g. insertions and deletions), copy-number variation and fusion transcripts.

 

Metagenomics refers to the study of genetic material recovered directly from ecological samples. Modern studies use either "shotgun" or PCR directed sequencing to get largely stable samples of all genes from all the members of the sampled populations. The aim of this approach is to recognize the genes and metabolic pathways that are existing.

 

Computational genomics is the combination of  both computational and statistical analysis to interpret biology from genome sequences and linked data, including both DNA and RNA sequence as well as other "post-genomic" data.  With the recent abundance of enormous biological datasets, computational studies have become one of the most important resources to biological discovery.

 

Cancer genomics refers to the study of the total DNA sequence and gene expression differences between tumour cells and normal host cells. Its objective is to understand the genetic basis of tumour cell proliferation and the growth of the cancer genome under mutation and selection by the body environment, the immune system and therapeutic interferences.

 

Molecular diagnostics explores how the genes and proteins are interacting inside a cell. The focus is on patterns--gene and protein activity patterns--in different types of cancerous or precancerous cells. The clinical science meeting aims to provide a rapid turn-around time possible for reviewing and publishing and to disseminate the articles freely for research, teaching and reference purposes.

 

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