Evidence map›Paper›PMID 39432565›Full record

ArticleBioinformatics (Oxford, England)2024

k-nonical space: sketching with reverse complements.

Guillaume Marçais, C S Elder, Carl Kingsford

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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. Regions Enriched with Reverse Complement Triplets in Bacterial Genomes.International journal of molecular sciences · 2026
    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

3 authors.

Guillaume MarçaisRay and Stephanie Lane Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA 15213, United States.ORCID 0000-0002-5083-5925
C S ElderRay and Stephanie Lane Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA 15213, United States.
Carl KingsfordRay and Stephanie Lane Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA 15213, United States.

Funding

Improved genomic sketching for MUMmer and metagenomicsR01HG012470 · NHGRI · CARNEGIE-MELLON UNIVERSITY · PI KINGSFORD, CARLETON LEE, MARÇAIS, GUILLAUME · 2022 to 2025
$1.7M
NHGRI NIH HHS R01 HG012470US National Science Foundation DBI-1937540
6 · The paper itself

Abstract

motivationSequences equivalent to their reverse complements (i.e. double-stranded DNA) have no analogue in text analysis and non-biological string algorithms. Despite this striking difference, algorithms designed for computational biology (e.g. sketching algorithms) are designed and tested in the same way as classical string algorithms. Then, as a post-processing step, these algorithms are adapted to work with genomic sequences by folding a k-mer and its reverse complement into a single sequence: The canonical representation (k-nonical space).

resultsThe effect of using the canonical representation with sketching methods is understudied and not understood. As a first step, we use context-free sketching methods to illustrate the potentially detrimental effects of using canonical k-mers with string algorithms not designed to accommodate for them. In particular, we show that large stretches of the genome ("sketching deserts") are undersampled or entirely skipped by context-free sketching methods, effectively making these genomic regions invisible to subsequent algorithms using these sketches. We provide empirical data showing these effects and develop a theoretical framework explaining the appearance of sketching deserts. Finally, we propose two schemes to accommodate for these effects: (i) a new procedure that adapts existing sketching methods to k-nonical space and (ii) an optimization procedure to directly design new sketching methods for k-nonical space. AVAILABILITY AND IMPLEMENTATION: The code used in this analysis is available under a permissive license at https://github.com/Kingsford-Group/mdsscope.

Indexed as

AlgorithmsComputational BiologyDNAGenomicsHumansSequence Analysis, DNADNA

Identifiers

PMID39432565
PMCPMC11549021

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.