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ISCN 2016: An International System for Human Cytogenomic Nomenclature (2016) Reprint of: Cytogenetic and Genome Research 2016, Vol. 149, No
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The 2016 edition of the International System for Human Cytogenomic Nomenclature (ISCN 2016) offers standard nomenclature that is used to describe any genomic rearrangement identified by techniques ranging from karyotyping to FISH, microarray, various region specific assays, and DNA sequencing. Suggestions from the international cytogenetics community have been reviewed by the Standing Committee, an international group of experts, nominated by their peers. This updated edition offers: many new examples, particularly for microarray and region specific assays trackable changes in the main text compared to the previous edition for easier identification a nomenclature standard to facilitate the description of chromosome rearrangements characterized by DNA sequencing developed through collaboration between the Human Genome Variation Society (HGVS) and ISCN to accommodate the increased use of sequencing technologies in the characterization of chromosomal abnormalities The ISCN 2016 is an indispensable reference volume for human cytogeneticists, molecular geneticists, technicians, and students for the interpretation and communication of human cytogenetic and molecular cytogenomic nomenclature. After a long collaboration with Cytogenetic and Genome Research, ISCN is now again a part of this leading journal on chromosome and genome research, combining the day-to-day business with the latest findings.
- Sales Rank: #367554 in Books
- Published on: 2016-05-11
- Original language: English
- Dimensions: 11.25" h x 8.50" w x .50" l,
- Binding: Paperback
- 140 pages
Most helpful customer reviews
0 of 0 people found the following review helpful.
An essential for those in the field, but not a significant update from the last edition
By Frank
Necessity for those in the field of cytogenetics. Not a whole lot of new material from the last update. Abnormal microarrays still do not specify gender while normal ones do...perhaps that can be rectified in a future edition. The major new change is incorporating sequence variants into the karyotype string, which may not be that useful in practice but is in line with ABMGs new approach to folding cytogenetics and molecular genetics into one combined specialty.
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