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BioFire Defense biofire fa-rp 2.1
Biofire Fa Rp 2.1, supplied by BioFire Defense, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/biofire+fa-rp+2%2E1/biofire+rp2+1/pm37797063-143-10-9
Average 90 stars, based on 1 article reviews
biofire fa-rp 2.1 - by Bioz Stars, 2026-09
90/100 stars

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MANN-WHITNEY:

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Similarly, among the patients who tested positive for the BioFire FA-RP 2.1, 9 years was the median age (Q1 3 –Q3 14), while those who tested negative had a median age of 4 years (Q1 0.8 –Q3 10); p = 0,001 U (Mann Whitney test).

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Several studies demonstrated the high sensitivity and specificity of BioFire FA-RP 2.1 in the adult population [18, 21–23].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 detected SARS-CoV-2 infection in 63 out of 339 (18.5%) nasopharyngeal swab samples obtained from the participants.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Our findings demonstrated the high sensitivity of BioFire FA-RP 2.1 for SARS-CoV-2 detection in children, a high positive likelihood ratio (LR+), and excellent agreement with the reference test.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 sensitivity was 95%, the specificity 94%, the positive predictive value 75%, and the negative predictive value 99%.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 automatically identifies the pathogen agent in the clinical sample, yielding immediate results, and boasts a rapid turnaround time of 45 minutes, faster than the conventional methods that can take over 4 hours.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: In addition to the BioFire FA-RP 2.1, several other rapid COVID-19 testing platforms have emerged, including the Cepheid Xpert Xpress SARS-CoV-2 [27], DiaSorin Simplexa [28, 29], and GenMark ePlex SARS-CoV-2 tests [30].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Here, we present the first prospective evaluation of the BioFire FA-RP 2.1 accuracy for SARS-CoV-2 detection in a pediatric population.

Infection:

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Similarly, among the patients who tested positive for the BioFire FA-RP 2.1, 9 years was the median age (Q1 3 –Q3 14), while those who tested negative had a median age of 4 years (Q1 0.8 –Q3 10); p = 0,001 U (Mann Whitney test).

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Several studies demonstrated the high sensitivity and specificity of BioFire FA-RP 2.1 in the adult population [18, 21–23].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 detected SARS-CoV-2 infection in 63 out of 339 (18.5%) nasopharyngeal swab samples obtained from the participants.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Our findings demonstrated the high sensitivity of BioFire FA-RP 2.1 for SARS-CoV-2 detection in children, a high positive likelihood ratio (LR+), and excellent agreement with the reference test.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 sensitivity was 95%, the specificity 94%, the positive predictive value 75%, and the negative predictive value 99%.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 automatically identifies the pathogen agent in the clinical sample, yielding immediate results, and boasts a rapid turnaround time of 45 minutes, faster than the conventional methods that can take over 4 hours.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: In addition to the BioFire FA-RP 2.1, several other rapid COVID-19 testing platforms have emerged, including the Cepheid Xpert Xpress SARS-CoV-2 [27], DiaSorin Simplexa [28, 29], and GenMark ePlex SARS-CoV-2 tests [30].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Here, we present the first prospective evaluation of the BioFire FA-RP 2.1 accuracy for SARS-CoV-2 detection in a pediatric population.

Reverse Transcription Polymerase Chain Reaction:

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Similarly, among the patients who tested positive for the BioFire FA-RP 2.1, 9 years was the median age (Q1 3 –Q3 14), while those who tested negative had a median age of 4 years (Q1 0.8 –Q3 10); p = 0,001 U (Mann Whitney test).

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Several studies demonstrated the high sensitivity and specificity of BioFire FA-RP 2.1 in the adult population [18, 21–23].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 detected SARS-CoV-2 infection in 63 out of 339 (18.5%) nasopharyngeal swab samples obtained from the participants.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Our findings demonstrated the high sensitivity of BioFire FA-RP 2.1 for SARS-CoV-2 detection in children, a high positive likelihood ratio (LR+), and excellent agreement with the reference test.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 sensitivity was 95%, the specificity 94%, the positive predictive value 75%, and the negative predictive value 99%.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 automatically identifies the pathogen agent in the clinical sample, yielding immediate results, and boasts a rapid turnaround time of 45 minutes, faster than the conventional methods that can take over 4 hours.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: In addition to the BioFire FA-RP 2.1, several other rapid COVID-19 testing platforms have emerged, including the Cepheid Xpert Xpress SARS-CoV-2 [27], DiaSorin Simplexa [28, 29], and GenMark ePlex SARS-CoV-2 tests [30].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Here, we present the first prospective evaluation of the BioFire FA-RP 2.1 accuracy for SARS-CoV-2 detection in a pediatric population.

Multiplex Assay:

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Similarly, among the patients who tested positive for the BioFire FA-RP 2.1, 9 years was the median age (Q1 3 –Q3 14), while those who tested negative had a median age of 4 years (Q1 0.8 –Q3 10); p = 0,001 U (Mann Whitney test).

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Several studies demonstrated the high sensitivity and specificity of BioFire FA-RP 2.1 in the adult population [18, 21–23].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 detected SARS-CoV-2 infection in 63 out of 339 (18.5%) nasopharyngeal swab samples obtained from the participants.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Our findings demonstrated the high sensitivity of BioFire FA-RP 2.1 for SARS-CoV-2 detection in children, a high positive likelihood ratio (LR+), and excellent agreement with the reference test.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 sensitivity was 95%, the specificity 94%, the positive predictive value 75%, and the negative predictive value 99%.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 automatically identifies the pathogen agent in the clinical sample, yielding immediate results, and boasts a rapid turnaround time of 45 minutes, faster than the conventional methods that can take over 4 hours.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: In addition to the BioFire FA-RP 2.1, several other rapid COVID-19 testing platforms have emerged, including the Cepheid Xpert Xpress SARS-CoV-2 [27], DiaSorin Simplexa [28, 29], and GenMark ePlex SARS-CoV-2 tests [30].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Here, we present the first prospective evaluation of the BioFire FA-RP 2.1 accuracy for SARS-CoV-2 detection in a pediatric population.

Polymerase Chain Reaction:

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Similarly, among the patients who tested positive for the BioFire FA-RP 2.1, 9 years was the median age (Q1 3 –Q3 14), while those who tested negative had a median age of 4 years (Q1 0.8 –Q3 10); p = 0,001 U (Mann Whitney test).

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Several studies demonstrated the high sensitivity and specificity of BioFire FA-RP 2.1 in the adult population [18, 21–23].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 detected SARS-CoV-2 infection in 63 out of 339 (18.5%) nasopharyngeal swab samples obtained from the participants.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Our findings demonstrated the high sensitivity of BioFire FA-RP 2.1 for SARS-CoV-2 detection in children, a high positive likelihood ratio (LR+), and excellent agreement with the reference test.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 sensitivity was 95%, the specificity 94%, the positive predictive value 75%, and the negative predictive value 99%.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: The BioFire FA-RP 2.1 automatically identifies the pathogen agent in the clinical sample, yielding immediate results, and boasts a rapid turnaround time of 45 minutes, faster than the conventional methods that can take over 4 hours.

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: In addition to the BioFire FA-RP 2.1, several other rapid COVID-19 testing platforms have emerged, including the Cepheid Xpert Xpress SARS-CoV-2 [27], DiaSorin Simplexa [28, 29], and GenMark ePlex SARS-CoV-2 tests [30].

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting.
Article Snippet: Here, we present the first prospective evaluation of the BioFire FA-RP 2.1 accuracy for SARS-CoV-2 detection in a pediatric population.



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Journal: PLOS ONE

Article Title: Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting

doi: 10.1371/journal.pone.0292314

Figure Lengend Snippet: Performance comparison between the BioFire FA-RP 2.1 and the reference RT-PCR tests according to the patient characteristics (positive testes, n = 111).

Article Snippet: To evaluate the accuracy of the BioFire FA-RP 2.1 Panel (BioFire Diagnostics, Salt Lake City, UT, USA), our index test, we utilized the Light Mix Modular SarbeCoV E-gene EAV kit (TIB Molbiol, Berlin, Germany) as the reference test for comparison.

Techniques: Comparison, Sampling