Evidence map›Paper›PMID 33694043›Full record

ArticleMolecular genetics and genomics : MGG2021

Performance comparison: exome sequencing as a single test replacing Sanger sequencing.

Hila Fridman, Concetta Bormans, Moshe Einhorn, Daniel Au, Arjan Bormans, Yuval Porat, Luisa Fernanda Sanchez, Brent Manning, Ephrat Levy-Lahad, Doron M Behar

Abstract read
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In one paragraph

Article in Molecular genetics and genomics : MGG, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
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

10 authors.

Hila FridmanMedical Genetics Institute, Shaare Zedek Medical Center, 91031, Jerusalem, Israel. hila.fridman@mail.huji.ac.il.ORCID http://orcid.org/0000-0002-1084-4800
Concetta BormansGenomic Research Center, Gene By Gene, Houston, TX, 77008, USA.
Moshe EinhornData Analysis Group, 6688218, Genoox, Tel Aviv, Israel.
Daniel AuGenomic Research Center, Gene By Gene, Houston, TX, 77008, USA.
Arjan BormansGenomic Research Center, Gene By Gene, Houston, TX, 77008, USA.
Yuval PoratData Analysis Group, 6688218, Genoox, Tel Aviv, Israel.
Luisa Fernanda SanchezGenomic Research Center, Gene By Gene, Houston, TX, 77008, USA.
Brent ManningGenomic Research Center, Gene By Gene, Houston, TX, 77008, USA.
Ephrat Levy-LahadMedical Genetics Institute, Shaare Zedek Medical Center, 91031, Jerusalem, Israel.
Doron M BeharGenomic Research Center, Gene By Gene, Houston, TX, 77008, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next generation sequencing tests are used routinely as first-choice tests in the clinic. However, systematic performance comparing the results of exome sequencing as a single test replacing Sanger sequencing of targeted gene(s) is still lacking. Performance comparison data are critically important for clinical case management. In this study, we compared Sanger-sequencing results of 258 genes to those obtained from next generation sequencing (NGS) using two exome-sequencing enrichment kits: Agilent-SureSelectQXT and Illumina-Nextera. Sequencing was performed on leukocytes and buccal-derived DNA from a single individual, and all 258 genes were sequenced a total of 11 times (using different sequencing methods and DNA sources). Sanger sequencing was completed for all exons, including flanking ± 8 bp regions. For the 258 genes, NGS mean coverage was > 20 × for > 98 and > 91% of the regions targeted by SureSelect and Nextera, respectively. Overall, 449 variants were identified in at least one experiment, and 407/449 (90.6%) were detected by all. Of the 42 discordant variants, 23 were determined as true calls, summing-up to a truth set of 430 variants. Sensitivity of true-variant detection was 99% for Sanger sequencing and 97-100% for the NGS experiments. Mean false-positive rates were 3.7E-6 for Sanger sequencing, 2.5E-6 for SureSelect-NGS and 5.2E-6 for Nextera-NGS. Our findings suggest a high overall concordance between Sanger sequencing and NGS performances. Both methods demonstrated false-positive and false-negative calls. High clinical suspicion for a specific diagnosis should, therefore, override negative results of either Sanger sequencing or NGS.

Indexed as

DNAExomeExome SequencingExonsGenetic VariationHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNADNAComparisonNext generationPerformanceSangerSequencing

Identifiers

What OpenQuestion holds

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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.