Kiko Garcia

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2 yrs

How RNA Sequencing is Revolutionizing Drug Discovery and Development | #rna Sequencing

How RNA Sequencing is Revolutionizing Drug Discovery and Development

How RNA Sequencing is Revolutionizing Drug Discovery and Development

RNA sequencing (RNA-Seq) is a high-throughput technology that was developed in 2008 for the study of the entire transcriptome. It can simultaneously measure the expression patterns of thousands of genes and provide insight into biological processes' functional pathways and regulat

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2 yrs

How to choose ANOVA? | # ANOVA

How to choose ANOVA?

How to choose ANOVA?

Analysis of variance (ANOVA) is a powerful statistical method that allows researchers to compare the means of two or more groups and determine if they are significantly different. It is a popular tool for testing hypotheses in a variety of fields in biology, including ecology, genetics, p

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2 yrs

How to choose ANOVA? | # ANOVA

How to choose ANOVA?

How to choose ANOVA?

Analysis of variance (ANOVA) is a powerful statistical method that allows researchers to compare the means of two or more groups and determine if they are significantly different. It is a popular tool for testing hypotheses in a variety of fields in biology, including ecology, genetics, p

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created a new article

2 yrs

Exploring How RNC-RNA Sequencing Illuminates Translational Dynamics and Molecular Mechanisms | # RNC-RNA Sequencing

Exploring How RNC-RNA Sequencing Illuminates Translational Dynamics and Molecular Mechanisms

Exploring How RNC-RNA Sequencing Illuminates Translational Dynamics and Molecular Mechanisms

When a ribosome is affixed to the polypeptide (protein) it is making, the ribosome-nascent chain complex (RNC) is the compilation of molecules that make up the ribosome. One of several methods can be used to halt the synthesis of the nascent polypeptide. RNCs are made and purified in labs

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2 yrs

How to Submit Sequence Data to GenBank | #sequence Data

How to Submit Sequence Data to GenBank

How to Submit Sequence Data to GenBank

Next-generation sequencing, PacBio SMRT sequencing, and Nanopore sequencing, can generate numerous sequence data in a single run. Raw reads or assembled sequence need to be submitted to public sequence repository (DDBJ/ENA/GenBank - INSDC), which is required by the overwhelming majority

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