Author: Robison Wells Publisher: Harper Collins ISBN: 0062093517 Category : Young Adult Fiction Languages : en Pages : 206
Book Description
Benson Fisher thought that a scholarship to Maxfield Academy would be the ticket out of his dead-end life. He was wrong. Now he’s trapped in a school that’s surrounded by a razor-wire fence. A school where video cameras monitor his every move. Where there are no adults. Where the kids have split into groups in order to survive. Where breaking the rules equals death. But when Benson stumbles upon the school’s real secret, he realizes that playing by the rules could spell a fate worse than death, and that escape—his only real hope for survival—may be impossible.
Author: Charlotte Ng Publisher: Springer Nature ISBN: 1071622935 Category : Science Languages : en Pages : 352
Book Description
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. Authoritative and cutting-edge, Variant Calling: Methods and Protocols aims to be a foundation for future studies and to be a source of inspiration for new investigations in the field.
Author: Conxi Lázaro Publisher: Academic Press ISBN: 0128205202 Category : Medical Languages : en Pages : 436
Book Description
Clinical DNA Variant Interpretation: Theory and Practice, a new volume in the Translational and Applied Genomics series, covers foundational aspects, modes of analysis, technology, disease and disorder specific case studies, and clinical integration. This book provides a deep theoretical background, as well as applied case studies and methodology, enabling researchers, clinicians and healthcare providers to effectively classify DNA variants associated with disease and patient phenotypes. Practical chapters discuss genomic variant interpretation, terminology and nomenclature, international consensus guidelines, population allele frequency, functional evidence transcripts for RNA, proteins, and enzymes, somatic mutations, somatic profiling, and much more. Compiles best practices, methods and sound evidence for DNA variant classification in one applied volume Features chapter contributions from international leaders in the field Includes practical examples of variant classification for common and rare disorders, and across clinical phenotypes
Author: Uwe Blumöhr Publisher: SAP PRESS ISBN: 9781592294008 Category : Computer integrated manufacturing systems Languages : en Pages : 0
Book Description
Need to know about Variant Configuration in SAP? Look no further. This is your complete resource to implementing, setting up, and using variant configuration with SAP ERP 6.0 and CRM 2007. Youll learn about the business processes and integration issues, details of configuration in SAP CRM, special features of industry solutions, extensions of SAP customers and partners, and the selected challenges of using variant configuration. The book provides real-world case studies and customer examples, so you can learn about the dos and donts of variant configuration projects in a business environment.
Author: Tim Weilkiens Publisher: Lulu.com ISBN: 3981787579 Category : Technology & Engineering Languages : en Pages : 100
Book Description
SysML does not provide explicit built-in language constructs to model variants. Nevertheless SysML is useful to create a model for variants. The VAMOS method presented in the book Variant Modeling with SysML is one option how to model variants with SysML. It uses the profile mechanism of SysML to extend the language with a concept for variant modeling. The concepts are core, variation point, variation, variant, variant constraint, and variant configuration. The book shows how to apply the concepts with standard SysML modeling tool. The book covers * Variant Modeling Concepts * Method for Variant Modeling with SysML (VAMOS) * Variant Stereotypes for SysML * Example: Forest Fire Detection System * Example: Virtual Museum Tour
Author: Susanne Winnacker Publisher: Penguin ISBN: 1101594438 Category : Young Adult Fiction Languages : en Pages : 215
Book Description
Tessa is a Variant, able to absorb the DNA of anyone she touches and mimic their appearance. Shunned by her family, she's spent the last two years training with the Forces with Extraordinary Abilities, a secret branch of the FBI. When a serial killer rocks a small town in Oregon, Tessa is given a mission: she must impersonate Madison, a local teen, to find the killer before he strikes again. Tessa hates everything about being an impostor—he stress, the danger, the deceit—but loves playing the role of a normal girl. Disguised as Madison, she finds friends, romance, and the kind of loving family she'd do anything to keep. Amid action, suspense, and a ticking clock, this superhuman arrives at a very human conclusion: even a girl who can look like anyone struggles the most with being herself.
Author: Annie Tsz Wai Chu Publisher: OAE Publishing Inc. ISBN: Category : Medical Languages : en Pages : 10
Book Description
Kindler Syndrome (KS) is one of the rarest subtypes of epidermolysis bullosa (EB). It is characterised by congenital blistering, skin fragility, photosensitivity, and poikilodermatous skin changes. It is an autosomal recessive condition with an established disease-causing mechanism of having biallelic pathogenic variants in the FERMT1 gene. Multiple variants have been reported worldwide since the discovery in 1954. This case report describes two patients of Chinese descent with molecularly confirmed KS, one diagnosed in infancy while the other in mid-adulthood. It highlights the importance and clinical utility of diagnosing KS in children versus adults. The identification of recurrent c.811C>T variant in both patients also expedited the review of local databases and the existing mutation spectrum KS in East Asians.
Author: Robison Wells
Author: World Health Organization
Author: Charlotte Ng
Author: Theodore Eliot Keats
Author: Conxi Lázaro
Author: Pragya Dhruv Yadav
Author: Uwe Blumöhr
Author: Tim Weilkiens
Author: Susanne Winnacker
Author: Annie Tsz Wai Chu