(-0.41%) 5 460.48 points
(-0.12%) 39 119 points
(-0.71%) 17 733 points
(-0.34%) $81.46
(-3.13%) $2.60
(0.01%) $2 336.90
(0.61%) $29.44
(0.28%) $1 009.00
(-0.06%) $0.933
(0.45%) $10.68
(-0.05%) $0.791
(0.86%) $85.73
Live Chart Being Loaded With Signals
Bionano Genomics, Inc. provides genome analysis software solutions. It offers Saphyr, a sample-to-result solution for structural variation analysis by optical genome mapping for genome analysis and understanding of genetic variation and function; Saphyr instrument, a single-molecule imager; Saphyr Chip, a consumable that packages the nanochannel arrays for DNA linearization; and Bionano Prep Kits and DNA labeling kits, which provide the reagents and protocols for extracting and labeling ultra-high molecular weight...
Stats | |
---|---|
Dagens volum | 1.59M |
Gjennomsnittsvolum | 1.31M |
Markedsverdi | 46.85M |
EPS | $-0.600 ( Q1 | 2024-05-08 ) |
Neste inntjeningsdato | ( $0 ) 2024-08-07 |
Last Dividend | $0 ( N/A ) |
Next Dividend | $0 ( N/A ) |
P/E |
-0.110 (Sector) 42.63 (Industry) 0 |
ATR14 | $0.00200 (0.29%) |
Date | Person | Action | Amount | type |
---|---|---|---|---|
2024-06-18 | Rajkovic Aleksandar | Buy | 30 000 | Stock Option (Right to Buy) |
2024-06-18 | Luderer Albert | Buy | 30 000 | Stock Option (Right to Buy) |
2024-06-18 | Vuori Kristiina Md | Buy | 30 000 | Stock Option (Right to Buy) |
2024-06-18 | Barker David L | Buy | 30 000 | Stock Option (Right to Buy) |
2024-06-18 | Wong Vincent Jung-fai | Buy | 30 000 | Stock Option (Right to Buy) |
INSIDER POWER |
---|
87.42 |
Last 99 transactions |
Buy: 19 833 960 | Sell: 808 309 |
Volum Korrelasjon
Bionano Genomics Inc Korrelasjon
10 Mest positive korrelasjoner | |
---|---|
OZEM | 1 |
VMAR | 0.91 |
JL | 0.906 |
FFIE | 0.896 |
CLNE | 0.893 |
NUVO | 0.892 |
WW | 0.892 |
ASLE | 0.89 |
EBTC | 0.882 |
AEHR | 0.881 |
10 Mest negative korrelasjoner | |
---|---|
ERNZ | -0.876 |
INDH | -0.869 |
NESR | -0.866 |
RFAIU | -0.863 |
PSTR | -0.855 |
BSCO | -0.853 |
VIA | -0.851 |
PPRUX | -0.848 |
DXJS | -0.835 |
OXSQ | -0.834 |
Visste du det?
Korrelasjon er en statistisk måling som beskriver forholdet mellom to variabler. Den varierer fra -1 til 1, hvor -1 indikerer en perfekt negativ korrelasjon (hvor en variabel øker, går den andre ned), 1 indikerer en perfekt positiv korrelasjon (hvor en variabel øker, går den andre også opp), og 0 indikerer ingen korrelasjon (det er ingen forhold mellom variablene).
Korrelasjon kan brukes til å analysere forholdet mellom to variabler, ikke bare aksjer. Det er vanligvis brukt innen områder som finans, økonomi, psykologi, og mer.
Bionano Genomics Inc Korrelasjon - Valuta/Råvare
Bionano Genomics Inc Økonomi
Annual | 2023 |
Omsetning: | $36.12M |
Bruttogevinst: | $9.57M (26.49 %) |
EPS: | $-6.81 |
FY | 2023 |
Omsetning: | $36.12M |
Bruttogevinst: | $9.57M (26.49 %) |
EPS: | $-6.81 |
FY | 2022 |
Omsetning: | $27.80M |
Bruttogevinst: | $5.95M (21.38 %) |
EPS: | $-4.58 |
FY | 2021 |
Omsetning: | $17.98M |
Bruttogevinst: | $3.87M (21.54 %) |
EPS: | $-0.260 |
Financial Reports:
No articles found.
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Bionano Genomics Inc
Bionano Genomics, Inc. provides genome analysis software solutions. It offers Saphyr, a sample-to-result solution for structural variation analysis by optical genome mapping for genome analysis and understanding of genetic variation and function; Saphyr instrument, a single-molecule imager; Saphyr Chip, a consumable that packages the nanochannel arrays for DNA linearization; and Bionano Prep Kits and DNA labeling kits, which provide the reagents and protocols for extracting and labeling ultra-high molecular weight. The company also provides Saphyr and Bionano compute servers; and NxClinical which offers one system for analysis and interpretation of genomic variants from microarray and next-generation sequencing data for cytogenetics and molecular genetics. In addition, it offers testing and laboratory services comprising FirstStepDx PLUS, a chromosomal microarray for identifying an underlying genetic cause in individuals with autism spectrum disorder, developmental delay, and intellectual disability; Fragile X syndrome (FXS) testing services; NextStepDx PLUS, a exome sequencing test to identify genetic variants that are associated with disorders of childhood development; EpiPanelDx PLUS, a genetic testing panel for patients who have experienced seizures, infantile spasms, encephalopathy, or febrile seizures; PGx test, which identifies over 60 alleles in 11 genes. The company was founded in 2003 and is headquartered in San Diego, California.
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