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Sequentia Biotech SL

Bellaterra, ES

Sequentia Biotech is a company founded in Spain aimng to empower research institutes and private companies in the fields of bioinformatics, biostatistics, biotechnologies, data management and R&D.

The availability of high-throughput technologies in molecular biology has created a huge gap between the production of data and its exploitation for basic and applied research. Sequentia Biotech merges this gap, thus easing scientific research, by providing a highly qualified and highly customizable consulting service spanning from the design of experiments to statistical analysis of data and its management.

Our services will make next-generation sequencing and scientific research more accessible and affordable for companies and institutes that are working in the fields of plant, human, animal and microbe genetics and molecular biology. Sequentia Biotech is also committed to joining national and international... Show more »

Sequentia Biotech is a company founded in Spain aimng to empower research institutes and private companies in the fields of bioinformatics, biostatistics, biotechnologies, data management and R&D.

The availability of high-throughput technologies in molecular biology has created a huge gap between the production of data and its exploitation for basic and applied research. Sequentia Biotech merges this gap, thus easing scientific research, by providing a highly qualified and highly customizable consulting service spanning from the design of experiments to statistical analysis of data and its management.

Our services will make next-generation sequencing and scientific research more accessible and affordable for companies and institutes that are working in the fields of plant, human, animal and microbe genetics and molecular biology. Sequentia Biotech is also committed to joining national and international projects engaged in improving agricultural sustainability through conservation, use and phenotypic and molecular characterization of neglected plant species.

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Artificial Intelligence RNA-Seq (A.I.R.)
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ChIP-Seq
Chromatin Immunoprecipitation Sequencing
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Chromatin Immunoprecipitation (ChIP) is an experimental technique used to investigate the interaction between proteins and DNA in the cell. It aims to determine whether specific proteins are associated with specific genomic regions, such as transcription factors on promoters or other DNA binding sites. ChIP also aims to determine... Show more »

Chromatin Immunoprecipitation (ChIP) is an experimental technique used to investigate the interaction between proteins and DNA in the cell. It aims to determine whether specific proteins are associated with specific genomic regions, such as transcription factors on promoters or other DNA binding sites. ChIP also aims to determine the specific location in the genome that various histone modifications are associated with, indicating the target of the histone modifiers. The immunoprecipitated DNA can be analysed either by Next-Generation Sequencing (ChIP-seq) or by hybridization on a microarray chip (ChIP-on-chip). With our pipelines we will be able to identify the binding sites of your proteins of interest and to quantify the changes among different samples.

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ChIP-ChIP
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Chromatin Immunoprecipitation (ChIP) is an experimental technique used to investigate the interaction between proteins and DNA in the cell. It aims to determine whether specific proteins are associated with specific genomic regions, such as transcription factors on promoters or other DNA binding sites. ChIP also aims to determine... Show more »

Chromatin Immunoprecipitation (ChIP) is an experimental technique used to investigate the interaction between proteins and DNA in the cell. It aims to determine whether specific proteins are associated with specific genomic regions, such as transcription factors on promoters or other DNA binding sites. ChIP also aims to determine the specific location in the genome that various histone modifications are associated with, indicating the target of the histone modifiers. The immunoprecipitated DNA can be analysed either by Next-Generation Sequencing (ChIP-seq) or by hybridization on a microarray chip (ChIP-on-chip). With our pipelines we will be able to identify the binding sites of your proteins of interest and to quantify the changes among different samples.

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RNA-Seq Data Analysis
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The transcriptome is the complete set of transcripts in a cell, tissue, or whole organism, for a specific developmental stage or physiological condition. Understanding the transcriptome is essential for interpreting the function of the genome and for understanding development and disease. RNA seq, also called “Whole Transcriptome... Show more »

The transcriptome is the complete set of transcripts in a cell, tissue, or whole organism, for a specific developmental stage or physiological condition. Understanding the transcriptome is essential for interpreting the function of the genome and for understanding development and disease. RNA seq, also called “Whole Transcriptome Shotgun Sequencing” (“WTSS”), refers to the use of high-throughput sequencing technologies to sequence cDNA in order to get information about a sample’s RNA content.

We offer to our customers RNA seq analyses on fully sequenced organisms as well as on non-sequenced ones.

With our RNA seq pipelines we are able to provide:
-Identification of the expressed genes
-Identification of splicing variants
-Determination of the gene structures
-Quantification of absolute and relative gene expression levels
-Relative expression of different alleles
-SNP discovery
-Detection of post-transcriptional edits
-De novo RNA sequencing

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Whole Genome Sequencing
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With our de novo sequencing pipelines we are able to provide:
-Generation of high-quality reference genome assemblies
-Structural and functional annotation of genes
-Identification and phylogenetic analysis of gene families (i.e. R-genes)
-Prediction of biosynthetic pathways

Whole genome sequencing is the process that... Show more »

With our de novo sequencing pipelines we are able to provide:
-Generation of high-quality reference genome assemblies
-Structural and functional annotation of genes
-Identification and phylogenetic analysis of gene families (i.e. R-genes)
-Prediction of biosynthetic pathways

Whole genome sequencing is the process that determines the complete DNA sequence of an organism’s genome at a single time. Almost any biological sample containing a full copy of the DNA can provide the genetic material necessary for full genome sequencing. De novo genome sequencing can be used to sequence uncharacterized genomes, if there is no reference sequence available, or known genomes if significant structural variation is expected.

De novo sequencing can be the first step toward the development of genetic and molecular tools and can speed up all further molecular analyses, such as the analysis of structural variations, exome sequencing, RNA-seq, DNA-methylation, ChIP-seq, molecular marker development, etc.

Thanks to parternships with european sequencing companies Sequentia Biotech can
offer high quality and affordable sequencing services on 454, Ion torrent, PacBIO and
Illumina platforms.

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Biology
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Biochemistry & Molecular Biology
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Biomolecular Interaction Analysis
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Protein-DNA Interaction Analysis
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Chromatin Immunoprecipitation (ChIP) Assays
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Nucleic Acid Services
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Nucleic Acid Analysis
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Nucleic Acid Data Analysis
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Sequencing Data Analysis
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DNA Services
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DNA Sequencing
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Next Generation Sequencing (NGS)
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