Variant

Introduction to SAP S4HANA Variant Configuration

MTO_UsingLO-VC

This volume provides practical guidance on a variety of techniques and steps to ensure successful variant calling. Chapters detail methods for variant calling from single-nucleotide variants to structural variants, variant calling in specialized data types such as RNA-seq and UMI-tagged sequencing, alignment-free genotyping and SNP calling, variant detection in single-cell DNA sequencing data, variant annotation, and preanalytical quality control to ensure successful variant calling. Written in the format of the highly successful Methods in Molecular Biology series, each chapter includes an introduction to the topic, lists step-by-step protocol to execute the algorithms, describes the input and output data, and includes tips on troubleshooting and known pitfalls.

BOM Classification Method

Now, you might be wondering why someone would write yet another book on SAP. SAP Variant Configuration has been a topic near and dear to my heart for many years. While there are other books out there on the topic, I never felt like they addressed the details I've learned the hard way for nearly 20 years. My goal is to impart everything I've learned to help you successfully model in Variant Configuration.
This book is both how to manual and a reference guide. The idea is that the initial sections of the book will provide you with a quick start guide to implementing a variant configuration model. Then I provide a walk through to see how the process will look for the user, and finally all the individual pieces of configuration and master data that make up the process.