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In webpack, all pre-processors need to be applied with a corresponding loader. vue-loader allows you to use other webpack loaders to process a part of a Vue component. It will automatically infer the proper loaders to use from the lang attribute of a language block.

For example, let's compile our <style> tag with Sass:

Under the hood, the text content inside the <style> tag will be first compiled by sass-loader before being passed on for further processing.

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Section for further information about how to configure vue-loader.

A common request is to be able to load a settings file in each component without the need to explicity import it each time, e.g. to use scss variables globally throughout all components. To accomplish this:

Then add the following webpack rule:

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It is recommended to only include variables, mixins, etc. in this file, to prevent duplicated css in your final, compiled files.

All JavaScript inside Vue components are processed by babel-loader by default. But you can of course change it:

Processing templates is a little different, because most webpack template loaders such as pug-loader return a template function instead of a compiled HTML string. Instead of using pug-loader , we can just install the original pug :

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If you intend to ship your Vue component as a reusable 3rd-party component, avoid using this syntax.

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Array-CGH

Mature B-cell neoplasms arise in B-cells that have entered germinal centers within lymph nodes as part of the immune response. They display great heterogeneity at the clinical, pathologic, and genetic levels and represent 6-7% and 5-6% of all new estimated cancer cases and deaths respectively in the US in 2009. They are the fifth most common neoplasm in both males and females, and of the 103,960 estimated new cases in 2009, 20,860 comprise diffuse large B-cell lymphoma (DLBCL), 20,580 multiple myeloma (MM), 15,490 chronic lymphocytic leukemia /small lymphocytic lymphoma (CLL/SLL), 14,900 follicular lymphoma (FL), 8,510 Hodgkin’s lymphoma (HL), 6,000 marginal zone lymphomas (MZL) (including the three subtypes: extranodal marginal zone of mucosa-associated lymphoid tissue [MALT], nodal marginal zone, and splenic marginal zone), and 3,730 mantle cell lymphomas (MCL), as the major subtypes. With the exclusion of HL, 32,520 deaths are expected in 2009 in the US as a result of these neoplasms.

Diagnosis of these neoplasms relies mostly on the pathologic examination of biopsy material, be it either of an incisional or excisional biopsy of a suspect lymph node, a fine needle aspirate of a suspect lymph node (as yet to be considered adequate for initial diagnosis, unless it is the only safe option), or a bone marrow aspirate. Unlike other cancers, rarely are other biopsy/surgical procedures performed prior to the initiation of treatment, thus limiting the amount of tissue available for diagnostic and prognostic purposes. CGI has optimized the utility of array-CGH so that it can be routinely applied to the study of a range of specimen types including formalin-fixed paraffin-embedded (FFPE) specimens, often the only specimen available for analysis.

CGI has designed an oligonucleotide-based array (MatBA®) for the detection of gains and losses in mature B-cell neoplasms for utilization within a clinical laboratory.

For CLL/SLL, it’s primary value is in routine prognostication, and as an assay, has been approved in the CGI Diagnostic Laboratory by both CLIA and New York State. In this disease where approximately 50% patients have an aggressive course and 50% can live for many years without requiring treatment, robust prognostication is highly desirable. Together with IGHV mutation status, theMatBA®-CLL Array-CGH test provides important genetic-based information to guide clinical management of this disease.

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Access this complimentary guide to learn how Group Policy and Hyper-V features and capabilities have changed in Windows Server 2016, and discover the key networking, security, and storage benefits these changes offer.

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