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If a strip of paper is folded repeatedly in half in the same direction, times, it will get folds, whose direction (left or right) is given by the pattern of 0's and 1's in the first terms of the regular paperfolding sequence. Opening out each fold to create a right-angled corner (or, equivalently, making a sequence of left and right turns ...
Paired-end tags (PET) (sometimes "Paired-End diTags", or simply "ditags") are the short sequences at the 5’ and 3' ends of a DNA fragment which are unique enough that they (theoretically) exist together only once in a genome, therefore making the sequence of the DNA in between them available upon search (if full-genome sequence data is available) or upon further sequencing (since tag sites ...
The first is called chromosome (or primer) walking and starts with sequencing the first piece. The next (contiguous) piece of the sequence is then sequenced using a primer which is complementary to the end of the first sequence read and so on. This technique doesn't require much assembling, but you need a lot of primers and it is relatively ...
December 7, 2017: Wray defends the FBI. Four months after Wray is sworn in as the eighth director of the FBI, he publicly defends the agency from Trump’s criticism of its role in investigating ...
On the morning of Dec. 26, 1996, John and Patsy Ramsey woke up to find their 6-year-old daughter, JonBenét Ramsey, missing from her bedroom. Shortly after, they found a handwritten ransom note ...
Dan Campbell is the NFL's most colorful head coach, so naturally, he found the perfect way to describe the end of the Lions' 11-game winning streak.
The idea of the look-and-say sequence is similar to that of run-length encoding. If started with any digit d from 0 to 9 then d will remain indefinitely as the last digit of the sequence. For any d other than 1, the sequence starts as follows: d, 1d, 111d, 311d, 13211d, 111312211d, 31131122211d, …
Most high-throughput, next generation sequencing platforms produce shorter read lengths compared to Sanger sequencing.These new platforms are able to generate large quantities of data in short periods of time, but until methods were developed for de novo assembly of large genomes from short read sequences, Sanger sequencing remained the standard method of creating a reference genome. [10]
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