Evidence map›Paper›PMID 26713687›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2016

Efficient Design of Compact Unstructured RNA Libraries Covering All k-mers.

Yaron Orenstein, Bonnie Berger

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Joker de Bruijn: Covering k-Mers Using Joker Characters.Journal of computational biology : a journal of computational molecular cell biology · 2018
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Yaron Orenstein1 Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology , Cambridge, MA.
Bonnie Berger1 Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology , Cambridge, MA.

Funding

Structure-Based Prediction of the InteractomeR01GM081871 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BERGER, BONNIE · 2008 to 2020
$4.3M
NIGMS NIH HHS R01 GM081871
6 · The paper itself

Abstract

Current microarray technologies to determine RNA structure or measure protein-RNA interactions rely on single-stranded, unstructured RNA probes on a chip covering together all k-mers. Since space on the array is limited, the problem is to efficiently design a compact library of unstructured ℓ-long RNA probes, where each k-mer is covered at least p times. Ray et al. designed such a library for specific values of k, ℓ, and p using ad-hoc rules. To our knowledge, there is no general method to date to solve this problem. Here, we address the problem of finding a minimum-size covering of all k-mers by ℓ-long sequences with the desired properties for any value of k, ℓ, and p. As we prove that the problem is NP-hard, we give two solutions: the first is a greedy algorithm with a logarithmic approximation ratio; the second, a heuristic greedy approach based on random walks in de Bruijn graphs. The heuristic algorithm works well in practice and produces a library of unstructured RNA probes that is only ∼1.1-times greater in size compared to the theoretical lower bound. We present results for typical values of k and probe lengths ℓ and show that our algorithm generates a library that is significantly smaller than the library of Ray et al.; moreover, we show that our algorithm outperforms naive methods. Our approach can be generalized and extended to generate RNA or DNA oligo libraries with other desired properties. The software is freely available online.

Indexed as

de Bruijn graphmicroarray library designRNA secondary structure

Identifiers

PMID26713687
PMCPMC4752187

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.