ShopSpell

Next-Generation Sequencing: Standard Operating Procedures and Applications [Hardcover]

$207.99       (Free Shipping)
72 available
  • Category: Books (Science)
  • ISBN-10:  1032392622
  • ISBN-10:  1032392622
  • ISBN-13:  9781032392622
  • ISBN-13:  9781032392622
  • Publisher:  CRC Press
  • Publisher:  CRC Press
  • Pages:  298
  • Pages:  298
  • Binding:  Hardcover
  • Binding:  Hardcover
  • SKU:  1032392622-11-MPOD
  • SKU:  1032392622-11-MPOD
  • Item ID: 107096711
  • Seller: ShopSpell
  • Ships in: 2 business days
  • Transit time: Up to 5 business days
  • Delivery by: Sep 29 to Oct 01
  • Notes: Brand New Book. Order Now.

1.???? Technologies, Computations and Data Analysis? for Next Generation Sequencing

2.???? Epigenetics: RNA-Seq, ChiP-Seq, MedIP-Seq and ATAC-Seq

3.???? Streamlining Next-Generation Sequencing Data Analysis with Nextflow and nf-core Pipelines

4.???? Best practices for variant calling using Genome Analysis Toolkit

5.???? Implementation of WGCNA for identifying regulatory modules in biological networks

6.???? Meta-analysis of RNA-seq and Microarray data

7.???? Best practices in single-cell RNA-seq data analysis

8.???? Integration of Spatial Transcriptomics and Single Cell RNA-Seq

9.???? Metagenomics Analysis Pipelines for Microbiome Studies: QIIME and Mothur

10.? Standard Operating Procedure and Applications in Single-Cell Transcriptomics

11.? Benchmarking and Evaluation of de novo Assembly Tools for Prokaryotic Long Reads from Oxford Nanopore Technologies

12.? Best Practices for Reproducible of Microbial Genomics Analysis

13.? Single Cell RNA-Seq Analyses in the Era of Artificial Intelligence

14.? Towards single-molecule protein sequencing

15.? SOPs on Effective Galaxy Workflows

16.? Motif prediction using ChIP-Seq data analysis using Galaxy

17.? Developing a Whole Exome Consensus Variant Calling Pipeline to Infer Causal Pathogenic Variants

Index

This reference book compiles standard operating procedures, protocols, and applications of Next-Generation Sequencing (NGS). It discusses genomic testing applications through NGS and protocols for cataloging variants of uncertain significance.

This cutting-edge reference book compiles standard operating procedures, protocols, and applications of next-glӎ