Natural stone and marble tiles vary in colour, shade and veining from piece to piece. Each stone has its own distinguishing characteristics due to the inherent variances caused by nature. This unique quality is an appealing factor and enhances the beauty of natural stone tiles. We recommend sealing natural stone. If you need further clarification on the variation involved please do not hesitate to contact us.
Our exquisite raised-relief decorative Prima line provides the highest quality, high fired Mexican ceramic tile in both gloss and matte finishes. These delightful, textured tiles are sometimes referred to as Malibu tile or Santa Barbara tile.
Our Prima high-relief tiles are each individually handmade using the ancient Spanish method called Cuerda Seca (Dry Cord). The artist first traces the design onto a blank tile, then painstakingly applies each color of paint using a bulb syringe. Once the design is perfect, the tile is then fired at high temperature to impart strength and durability.
The colors and designs coordinate with our Prima solid color tiles, trim tile, and Prima raised-relief border tile. They also coordinate well with many of our hand-painted Mexican ceramic sinks. These gorgeous textured tile are ideal for pools, fountains, bathroom countertops, showers and tub surrounds, kitchen counters and backsplashes, outdoor kitchens and barbecues, patios and almost anywhere else your want to add a delightful textured touch of color and design. Every tile is truly a colorful and tactile work of art that will add lasting beauty and warmth to your home.
*Note: Prima ceramic tile are perfect for both indoor and outdoor applications and are frost resistant but not frost-proof. If greater durability is required, most Prima tile are also available in porcelain, please call 866-320-1628 for prices and ordering.
Discover the elegance of Rosetta, a stunning porcelain tile featuring a Burlington stone effect in a contemporary dark grey colouring, perfect for enhancing your interior floors, with its square 600x600mm format, 8mm thickness, rectified edges and classy matt finish, Rosetta promises both style and durability for any modern space in mind.
Rosetta is a custom ASIC switch that implements Cray's Slingshot interconnect. Implemented on 16 nm and consuming around 250 W, Rosetta is a 64-port switch. Each port is 200 Gbps/dir implemented as a standard 4-lane PAM4 56G.
Rosetta uses a tiled architecture. There are 32 tiles in the center of the die and 32 additional tiles at the parameter. Each tile carries the functionality of two ports. The 32 tiles at the parameter of the die contain the peripheral functions containing the edge functionalities including the SerDes, Ethernet lookup functions, MAC/PCS/LLR, and others. In the center of the die are the 32 blocks with the remaining functionality.
Rosetta utilizes a tiled architecture organized as four rows of eight tiles. There are two switch ports per tile, therefore with 32 tiles, there are 64 ports. Rosetta is implemented as a hierarchical crossbar with distributed crossbars based on row busses, column channels, and per tile crossbar.
In other words, every port has its own row bus which communicates across its row. There is a set of eight-column channels that are connected to the eight ports within that column. Since there are two switch ports per tile, there are two of those eight-column channel sets. Per tile, there is a 16-input 8-output crossbar which does the corner turns to the four rows (with two ports per row tile, you need eight outputs in total).
For example, to go from Port18 to Port9, pockets are first routed from Port18 along the row-bus to the local crossbar on the 5th column. From the local crossbar, the pocket is then routed upward to Port9 along the column channels.
Within each tile is the 16:8 crossbar. Internally, the crossbar comprises 5 independent crossbars - requests to transmit, grants, request queue credits, data, and end-to-end acknowledgment. The chip relies on a virtual output queued architecture meaning the data comes to the input buffers and remains there until it's ready to be sent out. This allows for head-of-line (HOL) blocking
Rosetta Ice 600x600mm (60x60cm) is a White natural look external/outdoor 20mm (2cm) thick porcelain paver tile. These rectified R11 (anti-slip rating) porcelain slab tiles are hard wearing, stylish and a very popular choice adding that contemporary feel to outside living areas such as patios, drive/path ways and garden surroundings. Maintenance free and weather proof porcelain pavers are the luxury choice to acheive that inside look outside.
Our Standard Delivery Time is 2-7 Working Days, however we do offer other delivery options (Please call our sales team on 0161 706 0087 for more information). Once you have placed your order and received confirmation of acceptance, we will contact you within one working day to arrange delivery on a convenient date for yourself.
All items or complete orders over 499 qualify for FREE standard delivery.
Please see our delivery page for more information.
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We are wholeheartedly committed to ensuring we offer a customer experience of the highest standard, from the second you click on our website, to the minute a box arrives and beyond.
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There are many tile sets that can create non-periodic tilings, but those can typically also be used to create a periodic tiling. What makes Penrose tiles special is that they can only be used to produce non-periodic tilings.
These so-called prototiles are usually depicted with smooth edges, but in reality Penrose tiles have interlocking tabsand cut-outs like the pieces of a jigsaw puzzle. For convenience these deformations are often replacedwith matching rules, which ensure that the tiles are only connected in ways that guaranteea non-periodic tiling. (Otherwise, for instance, you could combine the kite and dart to form a rhombus,and easily create a periodic tiling from there.)
More commonly a method is used that takes advantage of the fact that Penrose tilings, like fractals,have a self-similarity on different levels. When zooming out it can be observed that groups of tiles are enclosed in areas thatform exactly the same pattern as the tiles on the lower level. Departing from an inflated level, the prototiles can besubdivided into smaller tiles, always observing the matching rules. The subdivision may have to be repeated several times, before the desired level of detail is reached. This process is called deflation.
In this page you can see and run the program(s) related to this task and their results. You can also change either the programs or the parameters they are called with, for experimentation, but remember that these programs were created with the main purpose of showing a clear solution of the task, and they generally lack any kind of validation.
Mosaic inlay jewelry is a signature style of Santo Domingo jewelers. Artists create mosaic inlay by attaching tiny gemstone tiles to a shell or gemstone base, forming colorful and unique patterns. The technique can be traced back to early forms of jewelry unearthed at Ancestral Puebloan (formerly referred to as Anasazi) sites throughout the Southwest, and many artists model their inlay designs after these early artifacts. Angie Reano Owen is credited with reviving the tradition of inlay jewelry in Santo Domingo Pueblo in the 1970s, and today Santo Domingo mosaic inlay is one of the jewelry styles most sought after by collectors of Native American art.
I'm loving the price of Vesdura flooring, but they seem to be exclusive to Build Direct with no real website. Has anyone used this flooring? Do you have problems with it? Bonus if you have pictures to show!! I'm liking Gibraltar, Plymouth, Rosetta, Fango, and Captiola. They are a mix of SPC and WPC. Thanks!
I used Vesdura on one of my projects. This is a mix of Capitola and Santa Cruz. First issue I had was after a couple months, the vinyl by the french doors warped because of the sun. That was my fault as I knew it had sun sensitivity, but thought it didn't get that much direct sun. I replaced that portion with tile. It also scratched when moving the couch. But, it was easy to install and looked good.
These tracks display the level of sequence uniqueness of the reference NCBI36/hg18genome assembly. They were generated using different window sizes, and high signalwill be found in areas where the sequence is unique.MethodsThe Broad alignability track displays whether a region is made up ofmostly unique or mostly non-unique sequence. To generate the track, every36-mer in the genome was marked as "unique" if the most similar 36-merelsewhere in the genome have at most 2 mismatches, and as "non-unique"otherwise. Position X in the alignable track is marked by 1 if >50% of thebases in [X-200,X+200] are "unique" and by 0 otherwise. Every point in thealignable track has a corresponding position in each of the ChIP signaltracks. The Broad alignability track was generated for the ENCODEproject as a tool for development of theBroad Histone tracks.The Duke uniqueness tracks display how unique is each sequence on thepositive strand starting at a particular base and of a particular length.Thus, the 20 bp track reflects the uniqueness of all 20 base sequences withthe score being assigned to the first base of the sequence. Scores arenormalized to between 0 and 1 with 1 representing a completely uniquesequence and 0 representing the sequence occurs >4 times in the genome(excluding chrN_random and alternative haplotypes). A score of 0.5indicates the sequence occurs exactly twice, likewise 0.33 for three timesand 0.25 for four times. The Duke uniqueness tracks were generatedfor the ENCODE project as tools in the development of theOpen Chromatin tracks.The Duke excluded regions track displays genomic regions forwhich mapped sequence tags were filtered out before signal generationand peak calling for Duke/UNC/UTA'sOpen Chromatin tracks.This track contains problematic regions for short sequence tag signaldetection (such as satellites and rRNA genes). TheDuke excluded regions track was generated for the ENCODE project.The Rosetta uniqueness track uses sequence 'tiles' of 35 bp.Each tile was aligned to the genome using the BWA aligner. Tiles that alignuniquely and perfectly in hg18 receive a p-value of 1e-37, while those thatalign perfectly in multiple locations receive a p-value of 0. For each tile,the oligo midpoint coordinate was recorded along with the -log_10 p-value:37 (unambiguous) to 0 (ambiguous). The Rosetta uniqueness track wasgenerated independently of the ENCODE project.The UMass uniqueness track displays a uniqueness signal for eachbase which represents the sum of both plus and minus strand 15-mer occurrencesof that particular 5'->3' (plus strand) sequence throughout the genome. Scoresare normalized between 0 and 1 by calculating ( 1 / N ) where N is the numberof genome wide occurrences of the 15-mer starting at position X. A score of 1represents a single genome wide occurrence of that 15-mer. A 0.5 wouldrepresent either 2 plus strand occurrences or 1 plus and 1 minus strandoccurrence, and so on. Ratios are rounded to 3 significant digits. Thereforea 0.000 would represent > 2000 occurrences. A 0 is reserved for a given 15-merthat is either not assembled or contains at least one N at position X. TheUMass uniqueness track was generated for the ENCODE project.The CRG Alignability tracks display how uniquely k-mer sequences alignto a region of the genome. To generate the data, the GEM-mappabilityprogram hasbeen employed. The method is equivalent to mapping sliding windows of k-mers(where k has been set to 36, 40, 50, 75 or 100 nts to produce these tracks)back to the genome using the GEM mapper aligner (up to 2 mismatches wereallowed in this case). For each window, a mapability score was computed(S = 1/(number of matches found in the genome): S=1 means one match in thegenome, S=0.5 is two matches in the genome, and so on). TheCRG Alignability tracks weregenerated independently of the ENCODE project, in the framework of the GEM(GEnome Multitool) project.CreditsThe Broad alignability track was created by the Broad Institute.Data generation and analysis was supported by funds from the NHGRI (the ENCODEproject), theBurroughs Wellcome Fund, Massachusetts General Hospital and the Broad Institute.The Duke uniqueness and Duke excluded regions tracks were createdby Terry Fureyand Debbie Winter at Duke Univerisity'sInstitute for Genome Sciences & Policy (IGSP);and Stefan Graf at theEuropean Bioinformatics Insitute (EBI).We thank NHGRI for ENCODE funding support.The Rosetta uniqueness track was created by John Castle, atRosetta Inpharmatics (Merck),with assistance from Melissa Cline at UCSC.The UMass uniqueness track was created by Bryan Lajoiein Job Dekker's Labat the University of Massachusetts Medical School. Funding Support: NIH grantHG003143 to JD. Keck Distinguished Young Scholar Award to JD. This track wasgenerated as part of the ENCODE project funded by the NHGRI.The CRG Alignability track was created by Thomas Derrien and PaoloRibeca in Roderic Guigo's lab at the Centre for GenomicRegulation (CRG), Barcelona, Spain. Thomas Derrien was supported by funds from NHGRI forthe ENCODE project, while Paolo Ribeca was funded by a Consolider grant CDS2007-00050from the Spanish Ministerio de Educacin y Ciencia.
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